Wikipedia:MeSH C16

From Wikipedia, the free encyclopedia

The following is a list of the "C" codes for MeSH. It is a product of the United States National Library of Medicine.

Source for content is here. (File "2006 MeSH Trees".)

Contents 1 MeSH C16 --- congenital, hereditary, and neonatal diseases and abnormalities 1.1 MeSH C16.131 --- abnormalities 1.1.1 MeSH C16.131.042 --- abnormalities, drug-induced 1.1.2 MeSH C16.131.077 --- abnormalities, multiple 1.1.3 MeSH C16.131.080 --- abnormalities, radiation-induced 1.1.4 MeSH C16.131.240 --- cardiovascular abnormalities 1.1.5 MeSH C16.131.260 --- chromosome disorders 1.1.6 MeSH C16.131.300 --- digeorge syndrome 1.1.7 MeSH C16.131.314 --- digestive system abnormalities 1.1.8 MeSH C16.131.384 --- eye abnormalities 1.1.9 MeSH C16.131.482 --- lymphatic abnormalities 1.1.10 MeSH C16.131.581 --- monsters 1.1.11 MeSH C16.131.621 --- musculoskeletal abnormalities 1.1.12 MeSH C16.131.666 --- nervous system malformations 1.1.13 MeSH C16.131.740 --- respiratory system abnormalities 1.1.14 MeSH C16.131.810 --- situs inversus 1.1.15 MeSH C16.131.831 --- skin abnormalities 1.1.16 MeSH C16.131.850 --- stomatognathic system abnormalities 1.1.17 MeSH C16.131.894 --- thyroid dysgenesis 1.1.18 MeSH C16.131.939 --- urogenital abnormalities 1.2 MeSH C16.300 --- fetal diseases 1.2.1 MeSH C16.300.030 --- chorioamnionitis 1.2.2 MeSH C16.300.060 --- erythroblastosis, fetal 1.2.3 MeSH C16.300.080 --- fetal alcohol syndrome 1.2.4 MeSH C16.300.100 --- fetal hypoxia 1.2.5 MeSH C16.300.390 --- fetal growth retardation 1.2.6 MeSH C16.300.570 --- fetal macrosomia 1.2.7 MeSH C16.300.580 --- meconium aspiration syndrome 1.3 MeSH C16.320 --- genetic diseases, inborn 1.3.1 MeSH C16.320.033 --- adrenal hyperplasia, congenital 1.3.2 MeSH C16.320.070 --- anemia, hemolytic, congenital 1.3.3 MeSH C16.320.077 --- anemia, hypoplastic, congenital 1.3.4 MeSH C16.320.080 --- ataxia telangiectasia 1.3.5 MeSH C16.320.099 --- blood coagulation disorders, inherited 1.3.6 MeSH C16.320.129 --- cadasil 1.3.7 MeSH C16.320.160 --- cardiomyopathy, hypertrophic, familial 1.3.8 MeSH C16.320.170 --- cherubism 1.3.9 MeSH C16.320.180 --- chromosome disorders 1.3.10 MeSH C16.320.190 --- cystic fibrosis 1.3.11 MeSH C16.320.240 --- dwarfism 1.3.12 MeSH C16.320.290 --- eye diseases, hereditary 1.3.13 MeSH C16.320.306 --- familial mediterranean fever 1.3.14 MeSH C16.320.322 --- genetic diseases, x-linked 1.3.15 MeSH C16.320.338 --- genetic diseases, y-linked 1.3.16 MeSH C16.320.355 --- hajdu-cheney syndrome 1.3.17 MeSH C16.320.365 --- hemoglobinopathies 1.3.18 MeSH C16.320.400 --- heredodegenerative disorders, nervous system 1.3.19 MeSH C16.320.427 --- hyperthyroxinemia, familial dysalbuminemic 1.3.20 MeSH C16.320.455 --- jervell-lange nielsen syndrome 1.3.21 MeSH C16.320.467 --- kallmann syndrome 1.3.22 MeSH C16.320.480 --- kartagener syndrome 1.3.23 MeSH C16.320.540 --- marfan syndrome 1.3.24 MeSH C16.320.565 --- metabolism, inborn errors 1.3.25 MeSH C16.320.577 --- muscular dystrophies 1.3.26 MeSH C16.320.590 --- myasthenic syndromes, congenital 1.3.27 MeSH C16.320.600 --- nail-patella syndrome 1.3.28 MeSH C16.320.700 --- neoplastic syndromes, hereditary 1.3.29 MeSH C16.320.737 --- osteogenesis imperfecta 1.3.30 MeSH C16.320.775 --- pain insensitivity, congenital 1.3.31 MeSH C16.320.800 --- romano-ward syndrome 1.3.32 MeSH C16.320.850 --- skin diseases, genetic 1.3.33 MeSH C16.320.925 --- werner syndrome 1.4 MeSH C16.614 --- infant, newborn, diseases 1.4.1 MeSH C16.614.042 --- amniotic band syndrome 1.4.2 MeSH C16.614.053 --- anemia, neonatal 1.4.3 MeSH C16.614.092 --- asphyxia neonatorum 1.4.4 MeSH C16.614.131 --- birth injuries 1.4.5 MeSH C16.614.213 --- cystic fibrosis 1.4.6 MeSH C16.614.258 --- epilepsy, benign neonatal 1.4.7 MeSH C16.614.304 --- erythroblastosis, fetal 1.4.8 MeSH C16.614.378 --- hemorrhagic disease of newborn 1.4.9 MeSH C16.614.390 --- hernia, umbilical 1.4.10 MeSH C16.614.414 --- hydrocephalus 1.4.11 MeSH C16.614.438 --- hydrophthalmos 1.4.12 MeSH C16.614.451 --- hyperbilirubinemia, neonatal 1.4.13 MeSH C16.614.465 --- hyperostosis, cortical, congenital 1.4.14 MeSH C16.614.492 --- ichthyosis 1.4.15 MeSH C16.614.521 --- infant, premature, diseases 1.4.16 MeSH C16.614.580 --- meconium aspiration syndrome 1.4.17 MeSH C16.614.595 --- mobius syndrome 1.4.18 MeSH C16.614.610 --- neonatal abstinence syndrome 1.4.19 MeSH C16.614.643 --- nystagmus, congenital 1.4.20 MeSH C16.614.677 --- ophthalmia neonatorum 1.4.21 MeSH C16.614.694 --- persistent fetal circulation syndrome 1.4.22 MeSH C16.614.716 --- persistent hyperinsulinemia hypoglycemia of infancy 1.4.23 MeSH C16.614.760 --- rothmund-thomson syndrome 1.4.24 MeSH C16.614.810 --- sclerema neonatorum 1.4.25 MeSH C16.614.815 --- severe combined immunodeficiency 1.4.26 MeSH C16.614.868 --- syphilis, congenital 1.4.27 MeSH C16.614.890 --- thanatophoric dysplasia 1.4.28 MeSH C16.614.909 --- toxoplasmosis, congenital 1.4.29 MeSH C16.614.947 --- wolman disease

[edit] MeSH C16 --- congenital, hereditary, and neonatal diseases and abnormalities

[edit] MeSH C16.131 --- abnormalities

[edit] MeSH C16.131.042 --- abnormalities, drug-induced

[edit] MeSH C16.131.077 --- abnormalities, multiple

• MeSH C16.131.077.065 --- alagille syndrome
• MeSH C16.131.077.095 --- angelman syndrome
• MeSH C16.131.077.112 --- bardet-biedl syndrome
• MeSH C16.131.077.130 --- basal cell nevus syndrome
• MeSH C16.131.077.133 --- beckwith-wiedemann syndrome
• MeSH C16.131.077.137 --- bloom syndrome
• MeSH C16.131.077.208 --- branchio-oto-renal syndrome
• MeSH C16.131.077.250 --- cockayne syndrome
• MeSH C16.131.077.262 --- cri-du-chat syndrome
• MeSH C16.131.077.272 --- de lange syndrome
• MeSH C16.131.077.327 --- down syndrome
• MeSH C16.131.077.350 --- ectodermal dysplasia
• MeSH C16.131.077.350.398 --- ellis-van creveld syndrome
• MeSH C16.131.077.350.424 --- focal dermal hypoplasia
• MeSH C16.131.077.350.712 --- neurocutaneous syndromes
• MeSH C16.131.077.393 --- gardner syndrome
• MeSH C16.131.077.410 --- holoprosencephaly
• MeSH C16.131.077.445 --- incontinentia pigmenti
• MeSH C16.131.077.509 --- laurence-moon syndrome
• MeSH C16.131.077.525 --- leopard syndrome
• MeSH C16.131.077.550 --- marfan syndrome
• MeSH C16.131.077.578 --- mobius syndrome
• MeSH C16.131.077.606 --- nail-patella syndrome
• MeSH C16.131.077.661 --- oculocerebrorenal syndrome
• MeSH C16.131.077.677 --- orofaciodigital syndromes
• MeSH C16.131.077.703 --- poems syndrome
• MeSH C16.131.077.730 --- prader-willi syndrome
• MeSH C16.131.077.740 --- proteus syndrome
• MeSH C16.131.077.745 --- prune belly syndrome
• MeSH C16.131.077.790 --- rubella syndrome, congenital
• MeSH C16.131.077.804 --- rubinstein-taybi syndrome
• MeSH C16.131.077.850 --- short rib-polydactyly syndrome
• MeSH C16.131.077.860 --- smith-lemli-opitz syndrome
• MeSH C16.131.077.938 --- waardenburg's syndrome
• MeSH C16.131.077.951 --- wolfram syndrome
• MeSH C16.131.077.970 --- zellweger syndrome

[edit] MeSH C16.131.080 --- abnormalities, radiation-induced

[edit] MeSH C16.131.240 --- cardiovascular abnormalities

• MeSH C16.131.240.110 --- arterio-arterial fistula
• MeSH C16.131.240.150 --- arteriovenous malformations
• MeSH C16.131.240.150.125 --- arteriovenous fistula
• MeSH C16.131.240.150.295 --- intracranial arteriovenous malformations
• MeSH C16.131.240.275 --- central nervous system vascular malformations
• MeSH C16.131.240.400 --- heart defects, congenital
• MeSH C16.131.240.400.090 --- aortic coarctation
• MeSH C16.131.240.400.145 --- arrhythmogenic right ventricular dysplasia
• MeSH C16.131.240.400.200 --- cor triatriatum
• MeSH C16.131.240.400.210 --- coronary vessel anomalies
• MeSH C16.131.240.400.220 --- crisscross heart
• MeSH C16.131.240.400.280 --- dextrocardia
• MeSH C16.131.240.400.280.500 --- kartagener syndrome
• MeSH C16.131.240.400.340 --- ductus arteriosus, patent
• MeSH C16.131.240.400.395 --- ebstein's anomaly
• MeSH C16.131.240.400.450 --- eisenmenger complex
• MeSH C16.131.240.400.560 --- heart septal defects
• MeSH C16.131.240.400.560.098 --- aortopulmonary septal defect
• MeSH C16.131.240.400.560.350 --- endocardial cushion defects
• MeSH C16.131.240.400.560.375 --- heart septal defects, atrial
• MeSH C16.131.240.400.560.375.518 --- lutembacher's syndrome
• MeSH C16.131.240.400.560.375.702 --- trilogy of fallot
• MeSH C16.131.240.400.560.540 --- heart septal defects, ventricular
• MeSH C16.131.240.400.625 --- hypoplastic left heart syndrome
• MeSH C16.131.240.400.685 --- leopard syndrome
• MeSH C16.131.240.400.701 --- levocardia
• MeSH C16.131.240.400.720 --- marfan syndrome
• MeSH C16.131.240.400.849 --- tetralogy of fallot
• MeSH C16.131.240.400.915 --- transposition of great vessels
• MeSH C16.131.240.400.915.300 --- double outlet right ventricle
• MeSH C16.131.240.400.920 --- tricuspid atresia
• MeSH C16.131.240.400.929 --- truncus arteriosus, persistent
• MeSH C16.131.240.670 --- pulmonary atresia
• MeSH C16.131.240.700 --- scimitar syndrome

[edit] MeSH C16.131.260 --- chromosome disorders

• MeSH C16.131.260.040 --- angelman syndrome
• MeSH C16.131.260.080 --- beckwith-wiedemann syndrome
• MeSH C16.131.260.090 --- branchio-oto-renal syndrome
• MeSH C16.131.260.190 --- cri-du-chat syndrome
• MeSH C16.131.260.210 --- de lange syndrome
• MeSH C16.131.260.260 --- down syndrome
• MeSH C16.131.260.380 --- holoprosencephaly
• MeSH C16.131.260.700 --- prader-willi syndrome
• MeSH C16.131.260.790 --- rubinstein-taybi syndrome
• MeSH C16.131.260.800 --- sex chromosome disorders
• MeSH C16.131.260.800.240 --- ectodermal dysplasia
• MeSH C16.131.260.800.240.350 --- focal dermal hypoplasia
• MeSH C16.131.260.800.300 --- fragile x syndrome
• MeSH C16.131.260.800.340 --- gonadal dysgenesis, 46,xy
• MeSH C16.131.260.800.345 --- gonadal dysgenesis, mixed
• MeSH C16.131.260.800.490 --- klinefelter syndrome
• MeSH C16.131.260.800.670 --- orofaciodigital syndromes
• MeSH C16.131.260.800.870 --- turner syndrome
• MeSH C16.131.260.940 --- wagr syndrome
• MeSH C16.131.260.970 --- williams syndrome

[edit] MeSH C16.131.300 --- digeorge syndrome

[edit] MeSH C16.131.314 --- digestive system abnormalities

• MeSH C16.131.314.094 --- anus, imperforate
• MeSH C16.131.314.125 --- biliary atresia
• MeSH C16.131.314.184 --- choledochal cyst
• MeSH C16.131.314.184.500 --- caroli disease
• MeSH C16.131.314.244 --- diaphragmatic eventration
• MeSH C16.131.314.330 --- esophageal atresia
• MeSH C16.131.314.439 --- hirschsprung disease
• MeSH C16.131.314.466 --- intestinal atresia
• MeSH C16.131.314.556 --- meckel diverticulum

[edit] MeSH C16.131.384 --- eye abnormalities

• MeSH C16.131.384.079 --- aniridia
• MeSH C16.131.384.079.950 --- wagr syndrome
• MeSH C16.131.384.159 --- anophthalmos
• MeSH C16.131.384.190 --- blepharophimosis
• MeSH C16.131.384.282 --- coloboma
• MeSH C16.131.384.405 --- ectopia lentis
• MeSH C16.131.384.480 --- hydrophthalmos
• MeSH C16.131.384.666 --- microphthalmos
• MeSH C16.131.384.784 --- retinal dysplasia

[edit] MeSH C16.131.482 --- lymphatic abnormalities

• MeSH C16.131.482.500 --- lymphangiectasis, intestinal

[edit] MeSH C16.131.581 --- monsters

• MeSH C16.131.581.197 --- anencephaly
• MeSH C16.131.581.806 --- twins, conjoined

[edit] MeSH C16.131.621 --- musculoskeletal abnormalities

• MeSH C16.131.621.077 --- arthrogryposis
• MeSH C16.131.621.207 --- craniofacial abnormalities
• MeSH C16.131.621.207.207 --- cleidocranial dysplasia
• MeSH C16.131.621.207.231 --- craniofacial dysostosis
• MeSH C16.131.621.207.231.427 --- hallermann's syndrome
• MeSH C16.131.621.207.231.480 --- hypertelorism
• MeSH C16.131.621.207.231.576 --- mandibulofacial dysostosis
• MeSH C16.131.621.207.231.576.410 --- goldenhar syndrome
• MeSH C16.131.621.207.240 --- craniosynostoses
• MeSH C16.131.621.207.240.100 --- acrocephalosyndactylia
• MeSH C16.131.621.207.410 --- holoprosencephaly
• MeSH C16.131.621.207.525 --- leopard syndrome
• MeSH C16.131.621.207.540 --- maxillofacial abnormalities
• MeSH C16.131.621.207.540.170 --- cherubism
• MeSH C16.131.621.207.540.460 --- jaw abnormalities
• MeSH C16.131.621.207.540.460.185 --- cleft palate
• MeSH C16.131.621.207.540.460.457 --- micrognathism
• MeSH C16.131.621.207.540.460.606 --- pierre robin syndrome
• MeSH C16.131.621.207.540.460.655 --- prognathism
• MeSH C16.131.621.207.540.460.813 --- retrognathism
• MeSH C16.131.621.207.620 --- microcephaly
• MeSH C16.131.621.207.690 --- noonan syndrome
• MeSH C16.131.621.207.700 --- orofaciodigital syndromes
• MeSH C16.131.621.207.715 --- plagiocephaly, nonsynostotic
• MeSH C16.131.621.207.720 --- platybasia
• MeSH C16.131.621.207.850 --- rubinstein-taybi syndrome
• MeSH C16.131.621.386 --- funnel chest
• MeSH C16.131.621.417 --- gastroschisis
• MeSH C16.131.621.445 --- hajdu-cheney syndrome
• MeSH C16.131.621.449 --- hip dislocation, congenital
• MeSH C16.131.621.551 --- klippel-feil syndrome
• MeSH C16.131.621.585 --- limb deformities, congenital
• MeSH C16.131.621.585.350 --- ectromelia
• MeSH C16.131.621.585.380 --- foot deformities, congenital
• MeSH C16.131.621.585.425 --- hand deformities, congenital
• MeSH C16.131.621.585.512 --- lower extremity deformities, congenital
• MeSH C16.131.621.585.600 --- polydactyly
• MeSH C16.131.621.585.600.750 --- short rib-polydactyly syndrome
• MeSH C16.131.621.585.620 --- proteus syndrome
• MeSH C16.131.621.585.800 --- syndactyly
• MeSH C16.131.621.585.800.100 --- acrocephalosyndactylia
• MeSH C16.131.621.585.800.756 --- poland syndrome
• MeSH C16.131.621.585.984 --- thanatophoric dysplasia
• MeSH C16.131.621.585.988 --- upper extremity deformities, congenital
• MeSH C16.131.621.906 --- synostosis
• MeSH C16.131.621.906.364 --- craniosynostoses
• MeSH C16.131.621.906.364.100 --- acrocephalosyndactylia
• MeSH C16.131.621.906.819 --- syndactyly
• MeSH C16.131.621.906.819.100 --- acrocephalosyndactylia
• MeSH C16.131.621.906.819.756 --- poland syndrome

[edit] MeSH C16.131.666 --- nervous system malformations

• MeSH C16.131.666.142 --- central nervous system cysts
• MeSH C16.131.666.142.100 --- arachnoid cysts
• MeSH C16.131.666.190 --- central nervous system vascular malformations
• MeSH C16.131.666.190.200 --- hemangioma, cavernous, central nervous system
• MeSH C16.131.666.190.600 --- central nervous system venous angioma
• MeSH C16.131.666.190.800 --- sinus pericranii
• MeSH C16.131.666.205 --- dandy-walker syndrome
• MeSH C16.131.666.300 --- hereditary motor and sensory neuropathies
• MeSH C16.131.666.300.200 --- charcot-marie-tooth disease
• MeSH C16.131.666.300.780 --- refsum disease
• MeSH C16.131.666.300.820 --- spastic paraplegia, hereditary
• MeSH C16.131.666.310 --- hereditary sensory and autonomic neuropathies
• MeSH C16.131.666.310.309 --- dysautonomia, familial
• MeSH C16.131.666.410 --- holoprosencephaly
• MeSH C16.131.666.450 --- hydranencephaly
• MeSH C16.131.666.460 --- intracranial arteriovenous malformations
• MeSH C16.131.666.680 --- neural tube defects
• MeSH C16.131.666.680.196 --- anencephaly
• MeSH C16.131.666.680.291 --- arnold-chiari malformation
• MeSH C16.131.666.680.488 --- encephalocele
• MeSH C16.131.666.680.598 --- meningocele
• MeSH C16.131.666.680.610 --- meningomyelocele
• MeSH C16.131.666.680.800 --- spinal dysraphism
• MeSH C16.131.666.680.800.730 --- spina bifida cystica
• MeSH C16.131.666.680.800.750 --- spina bifida occulta
• MeSH C16.131.666.845 --- septo-optic dysplasia

[edit] MeSH C16.131.740 --- respiratory system abnormalities

• MeSH C16.131.740.195 --- bronchogenic cyst
• MeSH C16.131.740.214 --- bronchopulmonary sequestration
• MeSH C16.131.740.271 --- choanal atresia
• MeSH C16.131.740.290 --- cystic adenomatoid malformation of lung, congenital
• MeSH C16.131.740.501 --- kartagener syndrome
• MeSH C16.131.740.815 --- scimitar syndrome
• MeSH C16.131.740.830 --- tracheobronchomegaly

[edit] MeSH C16.131.810 --- situs inversus

• MeSH C16.131.810.250 --- dextrocardia
• MeSH C16.131.810.250.500 --- kartagener syndrome
• MeSH C16.131.810.700 --- levocardia

[edit] MeSH C16.131.831 --- skin abnormalities

• MeSH C16.131.831.066 --- acrodermatitis
• MeSH C16.131.831.150 --- dyskeratosis congenita
• MeSH C16.131.831.350 --- ectodermal dysplasia
• MeSH C16.131.831.350.398 --- ellis-van creveld syndrome
• MeSH C16.131.831.350.424 --- focal dermal hypoplasia
• MeSH C16.131.831.350.712 --- neurocutaneous syndromes
• MeSH C16.131.831.428 --- ehlers-danlos syndrome
• MeSH C16.131.831.493 --- epidermolysis bullosa
• MeSH C16.131.831.493.080 --- epidermolysis bullosa acquisita
• MeSH C16.131.831.493.160 --- epidermolysis bullosa dystrophica
• MeSH C16.131.831.493.170 --- epidermolysis bullosa, junctional
• MeSH C16.131.831.493.180 --- epidermolysis bullosa simplex
• MeSH C16.131.831.512 --- ichthyosis
• MeSH C16.131.831.512.400 --- ichthyosiform erythroderma, congenital
• MeSH C16.131.831.512.400.375 --- hyperkeratosis, epidermolytic
• MeSH C16.131.831.512.400.410 --- ichthyosis, lamellar
• MeSH C16.131.831.512.410 --- ichthyosis vulgaris
• MeSH C16.131.831.512.420 --- ichthyosis, x-linked
• MeSH C16.131.831.512.723 --- sjogren-larsson syndrome
• MeSH C16.131.831.580 --- incontinentia pigmenti
• MeSH C16.131.831.675 --- port-wine stain
• MeSH C16.131.831.766 --- pseudoxanthoma elasticum
• MeSH C16.131.831.775 --- rothmund-thomson syndrome
• MeSH C16.131.831.812 --- sclerema neonatorum
• MeSH C16.131.831.936 --- xeroderma pigmentosum

[edit] MeSH C16.131.850 --- stomatognathic system abnormalities

• MeSH C16.131.850.500 --- maxillofacial abnormalities
• MeSH C16.131.850.500.460 --- jaw abnormalities
• MeSH C16.131.850.500.460.185 --- cleft palate
• MeSH C16.131.850.500.460.457 --- micrognathism
• MeSH C16.131.850.500.460.606 --- pierre robin syndrome
• MeSH C16.131.850.500.460.655 --- prognathism
• MeSH C16.131.850.500.460.813 --- retrognathism
• MeSH C16.131.850.525 --- mouth abnormalities
• MeSH C16.131.850.525.164 --- cleft lip
• MeSH C16.131.850.525.185 --- cleft palate
• MeSH C16.131.850.525.304 --- fibromatosis, gingival
• MeSH C16.131.850.525.480 --- macrostomia
• MeSH C16.131.850.525.520 --- microstomia
• MeSH C16.131.850.525.955 --- velopharyngeal insufficiency
• MeSH C16.131.850.800 --- tooth abnormalities
• MeSH C16.131.850.800.065 --- amelogenesis imperfecta
• MeSH C16.131.850.800.065.300 --- dental enamel hypoplasia
• MeSH C16.131.850.800.100 --- anodontia
• MeSH C16.131.850.800.250 --- dens in dente
• MeSH C16.131.850.800.260 --- dentin dysplasia
• MeSH C16.131.850.800.270 --- dentinogenesis imperfecta
• MeSH C16.131.850.800.370 --- fused teeth
• MeSH C16.131.850.800.600 --- odontodysplasia
• MeSH C16.131.850.800.850 --- tooth, supernumerary

[edit] MeSH C16.131.894 --- thyroid dysgenesis

• MeSH C16.131.894.500 --- lingual thyroid
• MeSH C16.131.894.500.500 --- lingual goiter

[edit] MeSH C16.131.939 --- urogenital abnormalities

• MeSH C16.131.939.132 --- bladder exstrophy
• MeSH C16.131.939.258 --- cryptorchidism
• MeSH C16.131.939.374 --- epispadias
• MeSH C16.131.939.445 --- frasier syndrome
• MeSH C16.131.939.516 --- hypospadias
• MeSH C16.131.939.629 --- multicystic dysplastic kidney
• MeSH C16.131.939.742 --- nephritis, hereditary
• MeSH C16.131.939.842 --- sex differentiation disorders
• MeSH C16.131.939.842.260 --- freemartinism
• MeSH C16.131.939.842.309 --- gonadal dysgenesis
• MeSH C16.131.939.842.309.193 --- gonadal dysgenesis, 46,xx
• MeSH C16.131.939.842.309.388 --- gonadal dysgenesis, 46,xy
• MeSH C16.131.939.842.309.391 --- gonadal dysgenesis, mixed
• MeSH C16.131.939.842.309.872 --- turner syndrome
• MeSH C16.131.939.842.316 --- hermaphroditism
• MeSH C16.131.939.842.316.313 --- hermaphroditism, true
• MeSH C16.131.939.842.316.627 --- pseudohermaphroditism
• MeSH C16.131.939.842.316.627.109 --- androgen-insensitivity syndrome
• MeSH C16.131.939.842.316.627.220 --- denys-drash syndrome
• MeSH C16.131.939.842.425 --- kallmann syndrome
• MeSH C16.131.939.842.454 --- klinefelter syndrome
• MeSH C16.131.939.921 --- wagr syndrome

[edit] MeSH C16.300 --- fetal diseases

[edit] MeSH C16.300.030 --- chorioamnionitis

[edit] MeSH C16.300.060 --- erythroblastosis, fetal

• MeSH C16.300.060.480 --- hydrops fetalis

[edit] MeSH C16.300.080 --- fetal alcohol syndrome

[edit] MeSH C16.300.100 --- fetal hypoxia

[edit] MeSH C16.300.390 --- fetal growth retardation

[edit] MeSH C16.300.570 --- fetal macrosomia

[edit] MeSH C16.300.580 --- meconium aspiration syndrome

[edit] MeSH C16.320 --- genetic diseases, inborn

[edit] MeSH C16.320.033 --- adrenal hyperplasia, congenital

[edit] MeSH C16.320.070 --- anemia, hemolytic, congenital

• MeSH C16.320.070.095 --- anemia, dyserythropoietic, congenital
• MeSH C16.320.070.100 --- anemia, hemolytic, congenital nonspherocytic
• MeSH C16.320.070.150 --- anemia, sickle cell
• MeSH C16.320.070.150.440 --- hemoglobin sc disease
• MeSH C16.320.070.150.670 --- sickle cell trait
• MeSH C16.320.070.365 --- elliptocytosis, hereditary
• MeSH C16.320.070.480 --- glucosephosphate dehydrogenase deficiency
• MeSH C16.320.070.480.370 --- favism
• MeSH C16.320.070.490 --- hemoglobin c disease
• MeSH C16.320.070.785 --- spherocytosis, hereditary
• MeSH C16.320.070.875 --- thalassemia
• MeSH C16.320.070.875.100 --- alpha-thalassemia
• MeSH C16.320.070.875.150 --- beta-thalassemia

[edit] MeSH C16.320.077 --- anemia, hypoplastic, congenital

• MeSH C16.320.077.090 --- anemia, diamond-blackfan
• MeSH C16.320.077.280 --- fanconi anemia

[edit] MeSH C16.320.080 --- ataxia telangiectasia

[edit] MeSH C16.320.099 --- blood coagulation disorders, inherited

• MeSH C16.320.099.037 --- activated protein c resistance
• MeSH C16.320.099.056 --- afibrinogenemia
• MeSH C16.320.099.075 --- antithrombin iii deficiency
• MeSH C16.320.099.080 --- bernard-soulier syndrome
• MeSH C16.320.099.300 --- factor v deficiency
• MeSH C16.320.099.310 --- factor vii deficiency
• MeSH C16.320.099.320 --- factor x deficiency
• MeSH C16.320.099.325 --- factor xi deficiency
• MeSH C16.320.099.330 --- factor xii deficiency
• MeSH C16.320.099.335 --- factor xiii deficiency
• MeSH C16.320.099.500 --- hemophilia a
• MeSH C16.320.099.510 --- hemophilia b
• MeSH C16.320.099.515 --- hermanski-pudlak syndrome
• MeSH C16.320.099.550 --- hypoprothrombinemias
• MeSH C16.320.099.690 --- protein c deficiency
• MeSH C16.320.099.820 --- thrombasthenia
• MeSH C16.320.099.900 --- von willebrand disease
• MeSH C16.320.099.970 --- wiskott-aldrich syndrome

[edit] MeSH C16.320.129 --- cadasil

[edit] MeSH C16.320.160 --- cardiomyopathy, hypertrophic, familial

[edit] MeSH C16.320.170 --- cherubism

[edit] MeSH C16.320.180 --- chromosome disorders

• MeSH C16.320.180.040 --- angelman syndrome
• MeSH C16.320.180.080 --- beckwith-wiedemann syndrome
• MeSH C16.320.180.090 --- branchio-oto-renal syndrome
• MeSH C16.320.180.190 --- cri-du-chat syndrome
• MeSH C16.320.180.210 --- de lange syndrome
• MeSH C16.320.180.260 --- down syndrome
• MeSH C16.320.180.380 --- holoprosencephaly
• MeSH C16.320.180.700 --- prader-willi syndrome
• MeSH C16.320.180.790 --- rubinstein-taybi syndrome
• MeSH C16.320.180.800 --- sex chromosome disorders
• MeSH C16.320.180.800.240 --- ectodermal dysplasia
• MeSH C16.320.180.800.240.350 --- focal dermal hypoplasia
• MeSH C16.320.180.800.300 --- fragile x syndrome
• MeSH C16.320.180.800.340 --- gonadal dysgenesis, 46,xy
• MeSH C16.320.180.800.345 --- gonadal dysgenesis, mixed
• MeSH C16.320.180.800.490 --- klinefelter syndrome
• MeSH C16.320.180.800.670 --- orofaciodigital syndromes
• MeSH C16.320.180.800.870 --- turner syndrome
• MeSH C16.320.180.940 --- wagr syndrome
• MeSH C16.320.180.970 --- williams syndrome

[edit] MeSH C16.320.190 --- cystic fibrosis

[edit] MeSH C16.320.240 --- dwarfism

• MeSH C16.320.240.500 --- achondroplasia
• MeSH C16.320.240.562 --- cockayne syndrome
• MeSH C16.320.240.625 --- congenital hypothyroidism
• MeSH C16.320.240.750 --- laron syndrome
• MeSH C16.320.240.875 --- mulibrey nanism

[edit] MeSH C16.320.290 --- eye diseases, hereditary

• MeSH C16.320.290.040 --- albinism
• MeSH C16.320.290.040.090 --- albinism, ocular
• MeSH C16.320.290.040.100 --- albinism, oculocutaneous
• MeSH C16.320.290.040.100.400 --- hermanski-pudlak syndrome
• MeSH C16.320.290.040.600 --- piebaldism
• MeSH C16.320.290.078 --- aniridia
• MeSH C16.320.290.078.950 --- wagr syndrome
• MeSH C16.320.290.142 --- choroideremia
• MeSH C16.320.290.162 --- corneal dystrophies, hereditary
• MeSH C16.320.290.162.410 --- fuchs' endothelial dystrophy
• MeSH C16.320.290.235 --- duane retraction syndrome
• MeSH C16.320.290.468 --- gyrate atrophy
• MeSH C16.320.290.564 --- optic atrophies, hereditary
• MeSH C16.320.290.564.400 --- optic atrophy, hereditary, leber
• MeSH C16.320.290.564.500 --- optic atrophy, autosomal dominant
• MeSH C16.320.290.564.980 --- wolfram syndrome
• MeSH C16.320.290.660 --- retinal dysplasia
• MeSH C16.320.290.684 --- retinitis pigmentosa
• MeSH C16.320.290.684.500 --- usher syndromes

[edit] MeSH C16.320.306 --- familial mediterranean fever

[edit] MeSH C16.320.322 --- genetic diseases, x-linked

• MeSH C16.320.322.061 --- androgen-insensitivity syndrome
• MeSH C16.320.322.092 --- choroideremia
• MeSH C16.320.322.108 --- dyskeratosis congenita
• MeSH C16.320.322.124 --- fabry disease
• MeSH C16.320.322.186 --- focal dermal hypoplasia
• MeSH C16.320.322.201 --- glycogen storage disease type iib
• MeSH C16.320.322.217 --- glycogen storage disease type viii
• MeSH C16.320.322.233 --- granulomatous disease, chronic
• MeSH C16.320.322.241 --- ichthyosis, x-linked
• MeSH C16.320.322.360 --- hemophilia b
• MeSH C16.320.322.500 --- mental retardation, x-linked
• MeSH C16.320.322.500.124 --- adrenoleukodystrophy
• MeSH C16.320.322.500.249 --- coffin-lowry syndrome
• MeSH C16.320.322.500.500 --- fragile x syndrome
• MeSH C16.320.322.500.625 --- lesch-nyhan syndrome
• MeSH C16.320.322.500.687 --- menkes kinky hair syndrome
• MeSH C16.320.322.500.750 --- mucopolysaccharidosis ii
• MeSH C16.320.322.500.875 --- pyruvate dehydrogenase complex deficiency disease
• MeSH C16.320.322.500.937 --- rett syndrome
• MeSH C16.320.322.562 --- muscular dystrophy, duchenne
• MeSH C16.320.322.625 --- muscular dystrophy, emery-dreifuss
• MeSH C16.320.322.750 --- oculocerebrorenal syndrome
• MeSH C16.320.322.906 --- pelizaeus-merzbacher disease
• MeSH C16.320.322.937 --- wiskott-aldrich syndrome

[edit] MeSH C16.320.338 --- genetic diseases, y-linked

[edit] MeSH C16.320.355 --- hajdu-cheney syndrome

[edit] MeSH C16.320.365 --- hemoglobinopathies

• MeSH C16.320.365.155 --- anemia, sickle cell
• MeSH C16.320.365.155.440 --- hemoglobin sc disease
• MeSH C16.320.365.155.668 --- sickle cell trait
• MeSH C16.320.365.463 --- hemoglobin c disease
• MeSH C16.320.365.826 --- thalassemia
• MeSH C16.320.365.826.100 --- alpha-thalassemia
• MeSH C16.320.365.826.100.350 --- hydrops fetalis
• MeSH C16.320.365.826.150 --- beta-thalassemia

[edit] MeSH C16.320.400 --- heredodegenerative disorders, nervous system

• MeSH C16.320.400.024 --- alexander disease
• MeSH C16.320.400.050 --- amyloid neuropathies, familial
• MeSH C16.320.400.150 --- canavan disease
• MeSH C16.320.400.200 --- cockayne syndrome
• MeSH C16.320.400.330 --- dystonia musculorum deformans
• MeSH C16.320.400.350 --- gerstmann-straussler-scheinker disease
• MeSH C16.320.400.375 --- hallervorden-spatz syndrome
• MeSH C16.320.400.387 --- hepatolenticular degeneration
• MeSH C16.320.400.393 --- hereditary central nervous system demyelinating diseases
• MeSH C16.320.400.400 --- hereditary motor and sensory neuropathies
• MeSH C16.320.400.400.200 --- charcot-marie-tooth disease
• MeSH C16.320.400.400.780 --- refsum disease
• MeSH C16.320.400.400.820 --- spastic paraplegia, hereditary
• MeSH C16.320.400.415 --- hereditary sensory and autonomic neuropathies
• MeSH C16.320.400.415.309 --- dysautonomia, familial
• MeSH C16.320.400.430 --- huntington disease
• MeSH C16.320.400.480 --- lafora disease
• MeSH C16.320.400.500 --- lesch-nyhan syndrome
• MeSH C16.320.400.520 --- menkes kinky hair syndrome
• MeSH C16.320.400.525 --- mental retardation, x-linked
• MeSH C16.320.400.525.124 --- adrenoleukodystrophy
• MeSH C16.320.400.525.249 --- coffin-lowry syndrome
• MeSH C16.320.400.525.500 --- fragile x syndrome
• MeSH C16.320.400.525.625 --- lesch-nyhan syndrome
• MeSH C16.320.400.525.687 --- menkes kinky hair syndrome
• MeSH C16.320.400.525.750 --- mucopolysaccharidosis ii
• MeSH C16.320.400.525.875 --- pyruvate dehydrogenase complex deficiency disease
• MeSH C16.320.400.525.937 --- rett syndrome
• MeSH C16.320.400.540 --- myotonia congenita
• MeSH C16.320.400.542 --- myotonic dystrophy
• MeSH C16.320.400.560 --- neurofibromatosis
• MeSH C16.320.400.560.400 --- neurofibromatosis 1
• MeSH C16.320.400.560.700 --- neurofibromatosis 2
• MeSH C16.320.400.600 --- neuronal ceroid-lipofuscinosis
• MeSH C16.320.400.630 --- optic atrophies, hereditary
• MeSH C16.320.400.630.400 --- optic atrophy, hereditary, leber
• MeSH C16.320.400.630.500 --- optic atrophy, autosomal dominant
• MeSH C16.320.400.630.980 --- wolfram syndrome
• MeSH C16.320.400.700 --- rett syndrome
• MeSH C16.320.400.765 --- spinal muscular atrophies of childhood
• MeSH C16.320.400.780 --- spinocerebellar degenerations
• MeSH C16.320.400.780.200 --- friedreich ataxia
• MeSH C16.320.400.780.500 --- myoclonic cerebellar dyssynergia
• MeSH C16.320.400.780.750 --- olivopontocerebellar atrophies
• MeSH C16.320.400.780.875 --- spinocerebellar ataxias
• MeSH C16.320.400.780.875.500 --- machado-joseph disease
• MeSH C16.320.400.820 --- tourette syndrome
• MeSH C16.320.400.880 --- tuberous sclerosis
• MeSH C16.320.400.940 --- unverricht-lundborg syndrome

[edit] MeSH C16.320.427 --- hyperthyroxinemia, familial dysalbuminemic

[edit] MeSH C16.320.455 --- jervell-lange nielsen syndrome

[edit] MeSH C16.320.467 --- kallmann syndrome

[edit] MeSH C16.320.480 --- kartagener syndrome

[edit] MeSH C16.320.540 --- marfan syndrome

[edit] MeSH C16.320.565 --- metabolism, inborn errors

• MeSH C16.320.565.066 --- amino acid metabolism, inborn errors
• MeSH C16.320.565.066.102 --- albinism
• MeSH C16.320.565.066.102.090 --- albinism, ocular
• MeSH C16.320.565.066.102.100 --- albinism, oculocutaneous
• MeSH C16.320.565.066.102.100.400 --- hermanski-pudlak syndrome
• MeSH C16.320.565.066.102.600 --- piebaldism
• MeSH C16.320.565.066.187 --- alkaptonuria
• MeSH C16.320.565.066.210 --- aminoaciduria, renal
• MeSH C16.320.565.066.210.250 --- cystinuria
• MeSH C16.320.565.066.210.490 --- hartnup disease
• MeSH C16.320.565.066.275 --- carbamoyl-phosphate synthase i deficiency disease
• MeSH C16.320.565.066.340 --- citrullinemia
• MeSH C16.320.565.066.470 --- homocystinuria
• MeSH C16.320.565.066.475 --- hyperargininemia
• MeSH C16.320.565.066.477 --- hyperglycinemia, nonketotic
• MeSH C16.320.565.066.480 --- hyperhomocysteinemia
• MeSH C16.320.565.066.544 --- hyperlysinemias
• MeSH C16.320.565.066.608 --- maple syrup urine disease
• MeSH C16.320.565.066.620 --- multiple carboxylase deficiency
• MeSH C16.320.565.066.620.100 --- biotinidase deficiency
• MeSH C16.320.565.066.620.380 --- holocarboxylase synthetase deficiency
• MeSH C16.320.565.066.729 --- ornithine carbamoyltransferase deficiency disease
• MeSH C16.320.565.066.766 --- phenylketonurias
• MeSH C16.320.565.066.766.500 --- phenylketonuria, maternal
• MeSH C16.320.565.066.880 --- tyrosinemias
• MeSH C16.320.565.088 --- amino acid transport disorders, inborn
• MeSH C16.320.565.088.400 --- hartnup disease
• MeSH C16.320.565.088.600 --- oculocerebrorenal syndrome
• MeSH C16.320.565.100 --- amyloidosis, familial
• MeSH C16.320.565.100.050 --- amyloid neuropathies, familial
• MeSH C16.320.565.100.160 --- cerebral amyloid angiopathy, familial
• MeSH C16.320.565.150 --- brain diseases, metabolic, inborn
• MeSH C16.320.565.150.050 --- abetalipoproteinemia
• MeSH C16.320.565.150.162 --- carbamoyl-phosphate synthase i deficiency disease
• MeSH C16.320.565.150.168 --- cerebral amyloid angiopathy, familial
• MeSH C16.320.565.150.175 --- citrullinemia
• MeSH C16.320.565.150.320 --- galactosemias
• MeSH C16.320.565.150.355 --- hartnup disease
• MeSH C16.320.565.150.360 --- hepatolenticular degeneration
• MeSH C16.320.565.150.365 --- homocystinuria
• MeSH C16.320.565.150.370 --- hyperargininemia
• MeSH C16.320.565.150.375 --- hyperglycinemia, nonketotic
• MeSH C16.320.565.150.380 --- hyperlysinemias
• MeSH C16.320.565.150.412 --- leigh disease
• MeSH C16.320.565.150.425 --- lesch-nyhan syndrome
• MeSH C16.320.565.150.435 --- lysosomal storage diseases, nervous system
• MeSH C16.320.565.150.435.295 --- fucosidosis
• MeSH C16.320.565.150.435.340 --- glycogen storage disease type ii
• MeSH C16.320.565.150.435.590 --- mucolipidoses
• MeSH C16.320.565.150.435.810 --- sialic acid storage disease
• MeSH C16.320.565.150.435.825 --- sphingolipidoses
• MeSH C16.320.565.150.435.825.200 --- fabry disease
• MeSH C16.320.565.150.435.825.300 --- gangliosidoses
• MeSH C16.320.565.150.435.825.300.300 --- gangliosidoses gm2
• MeSH C16.320.565.150.435.825.300.300.800 --- sandhoff disease
• MeSH C16.320.565.150.435.825.300.300.840 --- tay-sachs disease
• MeSH C16.320.565.150.435.825.300.300.920 --- tay-sachs disease, ab variant
• MeSH C16.320.565.150.435.825.300.400 --- gangliosidosis gm1
• MeSH C16.320.565.150.435.825.400 --- gaucher disease
• MeSH C16.320.565.150.435.825.590 --- leukodystrophy, globoid cell
• MeSH C16.320.565.150.435.825.594 --- leukodystrophy, metachromatic
• MeSH C16.320.565.150.435.825.700 --- niemann-pick diseases
• MeSH C16.320.565.150.520 --- maple syrup urine disease
• MeSH C16.320.565.150.535 --- melas syndrome
• MeSH C16.320.565.150.540 --- menkes kinky hair syndrome
• MeSH C16.320.565.150.545 --- merrf syndrome
• MeSH C16.320.565.150.640 --- oculocerebrorenal syndrome
• MeSH C16.320.565.150.650 --- ornithine carbamoyltransferase deficiency disease
• MeSH C16.320.565.150.680 --- peroxisomal disorders
• MeSH C16.320.565.150.680.100 --- adrenoleukodystrophy
• MeSH C16.320.565.150.680.760 --- refsum disease
• MeSH C16.320.565.150.680.970 --- zellweger syndrome
• MeSH C16.320.565.150.687 --- phenylketonurias
• MeSH C16.320.565.150.687.500 --- phenylketonuria, maternal
• MeSH C16.320.565.150.725 --- pyruvate carboxylase deficiency disease
• MeSH C16.320.565.150.750 --- pyruvate dehydrogenase complex deficiency disease
• MeSH C16.320.565.150.875 --- tyrosinemias
• MeSH C16.320.565.202 --- carbohydrate metabolism, inborn errors
• MeSH C16.320.565.202.125 --- carbohydrate-deficient glycoprotein syndrome
• MeSH C16.320.565.202.251 --- fructose metabolism, inborn errors
• MeSH C16.320.565.202.251.221 --- fructose-1,6-diphosphatase deficiency
• MeSH C16.320.565.202.251.271 --- fructose intolerance
• MeSH C16.320.565.202.303 --- fucosidosis
• MeSH C16.320.565.202.355 --- galactosemias
• MeSH C16.320.565.202.449 --- glycogen storage disease
• MeSH C16.320.565.202.449.448 --- glycogen storage disease type i
• MeSH C16.320.565.202.449.500 --- glycogen storage disease type ii
• MeSH C16.320.565.202.449.510 --- glycogen storage disease type iib
• MeSH C16.320.565.202.449.520 --- glycogen storage disease type iii
• MeSH C16.320.565.202.449.540 --- glycogen storage disease type iv
• MeSH C16.320.565.202.449.560 --- glycogen storage disease type v
• MeSH C16.320.565.202.449.580 --- glycogen storage disease type vi
• MeSH C16.320.565.202.449.600 --- glycogen storage disease type vii
• MeSH C16.320.565.202.449.620 --- glycogen storage disease type viii
• MeSH C16.320.565.202.460 --- hyperoxaluria, primary
• MeSH C16.320.565.202.589 --- lactose intolerance
• MeSH C16.320.565.202.607 --- mannosidase deficiency diseases
• MeSH C16.320.565.202.607.500 --- alpha-mannosidosis
• MeSH C16.320.565.202.607.750 --- beta-mannosidosis
• MeSH C16.320.565.202.670 --- mucolipidoses
• MeSH C16.320.565.202.715 --- mucopolysaccharidoses
• MeSH C16.320.565.202.715.640 --- mucopolysaccharidosis i
• MeSH C16.320.565.202.715.645 --- mucopolysaccharidosis ii
• MeSH C16.320.565.202.715.650 --- mucopolysaccharidosis iii
• MeSH C16.320.565.202.715.655 --- mucopolysaccharidosis iv
• MeSH C16.320.565.202.715.670 --- mucopolysaccharidosis vi
• MeSH C16.320.565.202.715.675 --- mucopolysaccharidosis vii
• MeSH C16.320.565.202.720 --- multiple carboxylase deficiency
• MeSH C16.320.565.202.720.100 --- biotinidase deficiency
• MeSH C16.320.565.202.720.380 --- holocarboxylase synthetase deficiency
• MeSH C16.320.565.202.742 --- nesidioblastosis
• MeSH C16.320.565.202.765 --- persistent hyperinsulinemia hypoglycemia of infancy
• MeSH C16.320.565.202.810 --- pyruvate metabolism, inborn errors
• MeSH C16.320.565.202.810.444 --- leigh disease
• MeSH C16.320.565.202.810.666 --- pyruvate carboxylase deficiency disease
• MeSH C16.320.565.202.810.766 --- pyruvate dehydrogenase complex deficiency disease
• MeSH C16.320.565.240 --- cytochrome-c oxidase deficiency
• MeSH C16.320.565.390 --- glucosephosphate dehydrogenase deficiency
• MeSH C16.320.565.437 --- hyperbilirubinemia, hereditary
• MeSH C16.320.565.437.281 --- crigler-najjar syndrome
• MeSH C16.320.565.437.528 --- gilbert disease
• MeSH C16.320.565.499 --- jaundice, chronic idiopathic
• MeSH C16.320.565.556 --- lipid metabolism, inborn errors
• MeSH C16.320.565.556.475 --- hypercholesterolemia, familial
• MeSH C16.320.565.556.480 --- hyperlipidemia, familial combined
• MeSH C16.320.565.556.480.390 --- hypercholesterolemia, familial
• MeSH C16.320.565.556.480.395 --- hyperlipoproteinemia type iv
• MeSH C16.320.565.556.483 --- hyperlipoproteinemia type iii
• MeSH C16.320.565.556.487 --- hyperlipoproteinemia type iv
• MeSH C16.320.565.556.493 --- hyperlipoproteinemia type v
• MeSH C16.320.565.556.500 --- hypolipoproteinemia
• MeSH C16.320.565.556.500.220 --- abetalipoproteinemia
• MeSH C16.320.565.556.500.440 --- hypobetalipoproteinemia
• MeSH C16.320.565.556.500.448 --- lecithin acyltransferase deficiency
• MeSH C16.320.565.556.500.724 --- tangier disease
• MeSH C16.320.565.556.641 --- lipoidosis
• MeSH C16.320.565.556.641.201 --- cholesterol ester storage disease
• MeSH C16.320.565.556.641.391 --- lipoidproteinosis
• MeSH C16.320.565.556.641.509 --- neuronal ceroid-lipofuscinosis
• MeSH C16.320.565.556.641.643 --- refsum disease
• MeSH C16.320.565.556.641.723 --- sjogren-larsson syndrome
• MeSH C16.320.565.556.641.803 --- sphingolipidoses
• MeSH C16.320.565.556.641.803.300 --- fabry disease
• MeSH C16.320.565.556.641.803.350 --- gangliosidoses
• MeSH C16.320.565.556.641.803.350.300 --- gangliosidoses gm2
• MeSH C16.320.565.556.641.803.350.300.700 --- sandhoff disease
• MeSH C16.320.565.556.641.803.350.300.850 --- tay-sachs disease
• MeSH C16.320.565.556.641.803.350.300.925 --- tay-sachs disease, ab variant
• MeSH C16.320.565.556.641.803.350.360 --- gangliosidosis gm1
• MeSH C16.320.565.556.641.803.441 --- gaucher disease
• MeSH C16.320.565.556.641.803.585 --- leukodystrophy, globoid cell
• MeSH C16.320.565.556.641.803.594 --- leukodystrophy, metachromatic
• MeSH C16.320.565.556.641.803.730 --- niemann-pick diseases
• MeSH C16.320.565.556.641.803.850 --- sea-blue histiocyte syndrome
• MeSH C16.320.565.556.641.923 --- wolman disease
• MeSH C16.320.565.556.645 --- lipoprotein lipase deficiency, familial
• MeSH C16.320.565.556.750 --- peroxisomal disorders
• MeSH C16.320.565.556.750.025 --- acatalasia
• MeSH C16.320.565.556.750.112 --- adrenoleukodystrophy
• MeSH C16.320.565.556.750.200 --- chondrodysplasia punctata, rhizomelic
• MeSH C16.320.565.556.750.760 --- refsum disease
• MeSH C16.320.565.556.750.970 --- zellweger syndrome
• MeSH C16.320.565.556.850 --- smith-lemli-opitz syndrome
• MeSH C16.320.565.556.925 --- xanthomatosis, cerebrotendinous
• MeSH C16.320.565.580 --- lysosomal storage diseases
• MeSH C16.320.565.580.201 --- cholesterol ester storage disease
• MeSH C16.320.565.580.554 --- lysosomal storage diseases, nervous system
• MeSH C16.320.565.580.554.295 --- fucosidosis
• MeSH C16.320.565.580.554.340 --- glycogen storage disease type ii
• MeSH C16.320.565.580.554.590 --- mucolipidoses
• MeSH C16.320.565.580.554.810 --- sialic acid storage disease
• MeSH C16.320.565.580.554.825 --- sphingolipidoses
• MeSH C16.320.565.580.554.825.200 --- fabry disease
• MeSH C16.320.565.580.554.825.300 --- gangliosidoses
• MeSH C16.320.565.580.554.825.300.300 --- gangliosidoses gm2
• MeSH C16.320.565.580.554.825.300.300.800 --- sandhoff disease
• MeSH C16.320.565.580.554.825.300.300.840 --- tay-sachs disease
• MeSH C16.320.565.580.554.825.300.300.920 --- tay-sachs disease, ab variant
• MeSH C16.320.565.580.554.825.300.400 --- gangliosidosis gm1
• MeSH C16.320.565.580.554.825.400 --- gaucher disease
• MeSH C16.320.565.580.554.825.590 --- leukodystrophy, globoid cell
• MeSH C16.320.565.580.554.825.594 --- leukodystrophy, metachromatic
• MeSH C16.320.565.580.554.825.700 --- niemann-pick diseases
• MeSH C16.320.565.580.577 --- mannosidase deficiency diseases
• MeSH C16.320.565.580.577.500 --- alpha-mannosidosis
• MeSH C16.320.565.580.577.750 --- beta-mannosidosis
• MeSH C16.320.565.580.600 --- mucopolysaccharidoses
• MeSH C16.320.565.580.600.640 --- mucopolysaccharidosis i
• MeSH C16.320.565.580.600.645 --- mucopolysaccharidosis ii
• MeSH C16.320.565.580.600.650 --- mucopolysaccharidosis iii
• MeSH C16.320.565.580.600.655 --- mucopolysaccharidosis iv
• MeSH C16.320.565.580.600.670 --- mucopolysaccharidosis vi
• MeSH C16.320.565.580.600.675 --- mucopolysaccharidosis vii
• MeSH C16.320.565.580.803 --- sphingolipidoses
• MeSH C16.320.565.580.803.300 --- fabry disease
• MeSH C16.320.565.580.803.350 --- gangliosidoses
• MeSH C16.320.565.580.803.350.300 --- gangliosidoses gm2
• MeSH C16.320.565.580.803.350.300.700 --- sandhoff disease
• MeSH C16.320.565.580.803.350.300.850 --- tay-sachs disease
• MeSH C16.320.565.580.803.350.300.925 --- tay-sachs disease, ab variant
• MeSH C16.320.565.580.803.441 --- gaucher disease
• MeSH C16.320.565.580.803.585 --- leukodystrophy, globoid cell
• MeSH C16.320.565.580.803.594 --- leukodystrophy, metachromatic
• MeSH C16.320.565.580.803.730 --- niemann-pick diseases
• MeSH C16.320.565.580.803.850 --- sea-blue histiocyte syndrome
• MeSH C16.320.565.580.923 --- wolman disease
• MeSH C16.320.565.618 --- metal metabolism, inborn errors
• MeSH C16.320.565.618.337 --- hemochromatosis
• MeSH C16.320.565.618.403 --- hepatolenticular degeneration
• MeSH C16.320.565.618.482 --- hypophosphatasia
• MeSH C16.320.565.618.544 --- hypophosphatemia, familial
• MeSH C16.320.565.618.590 --- menkes kinky hair syndrome
• MeSH C16.320.565.618.711 --- paralyses, familial periodic
• MeSH C16.320.565.618.711.550 --- hypokalemic periodic paralysis
• MeSH C16.320.565.618.711.600 --- paralysis, hyperkalemic periodic
• MeSH C16.320.565.618.711.600.500 --- andersen syndrome
• MeSH C16.320.565.618.815 --- pseudohypoparathyroidism
• MeSH C16.320.565.618.815.815 --- pseudopseudohypoparathyroidism
• MeSH C16.320.565.731 --- porphyria, erythropoietic
• MeSH C16.320.565.735 --- porphyrias, hepatic
• MeSH C16.320.565.735.074 --- coproporphyria, hereditary
• MeSH C16.320.565.735.150 --- porphyria, acute intermittent
• MeSH C16.320.565.735.250 --- porphyria cutanea tarda
• MeSH C16.320.565.735.437 --- porphyria, hepatoerythropoietic
• MeSH C16.320.565.735.625 --- porphyria, variegate
• MeSH C16.320.565.735.812 --- protoporphyria, erythropoietic
• MeSH C16.320.565.769 --- progeria
• MeSH C16.320.565.798 --- purine-pyrimidine metabolism, inborn errors
• MeSH C16.320.565.798.368 --- gout
• MeSH C16.320.565.798.368.410 --- arthritis, gouty
• MeSH C16.320.565.798.594 --- lesch-nyhan syndrome
• MeSH C16.320.565.851 --- renal tubular transport, inborn errors
• MeSH C16.320.565.851.093 --- acidosis, renal tubular
• MeSH C16.320.565.851.191 --- aminoaciduria, renal
• MeSH C16.320.565.851.191.250 --- cystinuria
• MeSH C16.320.565.851.191.457 --- hartnup disease
• MeSH C16.320.565.851.368 --- cystinosis
• MeSH C16.320.565.851.368.210 --- fanconi syndrome
• MeSH C16.320.565.851.532 --- glycosuria, renal
• MeSH C16.320.565.851.647 --- hypophosphatemia, familial
• MeSH C16.320.565.851.750 --- oculocerebrorenal syndrome
• MeSH C16.320.565.851.770 --- pseudohypoaldosteronism
• MeSH C16.320.565.925 --- steroid metabolism, inborn errors
• MeSH C16.320.565.925.249 --- adrenal hyperplasia, congenital
• MeSH C16.320.565.925.500 --- mineralocorticoid excess syndrome, apparent
• MeSH C16.320.565.925.750 --- ichthyosis, x-linked
• MeSH C16.320.565.925.875 --- smith-lemli-opitz syndrome

[edit] MeSH C16.320.577 --- muscular dystrophies

• MeSH C16.320.577.074 --- distal myopathies
• MeSH C16.320.577.149 --- glycogen storage disease type vii
• MeSH C16.320.577.280 --- muscular dystrophies, limb-girdle
• MeSH C16.320.577.300 --- muscular dystrophy, duchenne
• MeSH C16.320.577.350 --- muscular dystrophy, emery-dreifuss
• MeSH C16.320.577.400 --- muscular dystrophy, facioscapulohumeral
• MeSH C16.320.577.450 --- muscular dystrophy, oculopharyngeal
• MeSH C16.320.577.500 --- myotonic dystrophy

[edit] MeSH C16.320.590 --- myasthenic syndromes, congenital

[edit] MeSH C16.320.600 --- nail-patella syndrome

[edit] MeSH C16.320.700 --- neoplastic syndromes, hereditary

• MeSH C16.320.700.100 --- adenomatous polyposis coli
• MeSH C16.320.700.100.393 --- gardner syndrome
• MeSH C16.320.700.175 --- basal cell nevus syndrome
• MeSH C16.320.700.250 --- colorectal neoplasms, hereditary nonpolyposis
• MeSH C16.320.700.305 --- dysplastic nevus syndrome
• MeSH C16.320.700.330 --- exostoses, multiple hereditary
• MeSH C16.320.700.435 --- hamartoma syndrome, multiple
• MeSH C16.320.700.600 --- li-fraumeni syndrome
• MeSH C16.320.700.630 --- multiple endocrine neoplasia
• MeSH C16.320.700.630.500 --- multiple endocrine neoplasia type 1
• MeSH C16.320.700.630.505 --- multiple endocrine neoplasia type 2a
• MeSH C16.320.700.630.510 --- multiple endocrine neoplasia type 2b
• MeSH C16.320.700.642 --- wilms tumor
• MeSH C16.320.700.642.220 --- denys-drash syndrome
• MeSH C16.320.700.642.950 --- wagr syndrome
• MeSH C16.320.700.645 --- Neurofibromatosis
• MeSH C16.320.700.645.650 --- neurofibromatosis 1
• MeSH C16.320.700.645.655 --- neurofibromatosis 2
• MeSH C16.320.700.705 --- peutz-jeghers syndrome
• MeSH C16.320.700.852 --- sturge-weber syndrome

[edit] MeSH C16.320.737 --- osteogenesis imperfecta

[edit] MeSH C16.320.775 --- pain insensitivity, congenital

[edit] MeSH C16.320.800 --- romano-ward syndrome

[edit] MeSH C16.320.850 --- skin diseases, genetic

• MeSH C16.320.850.080 --- albinism
• MeSH C16.320.850.080.090 --- albinism, ocular
• MeSH C16.320.850.080.100 --- albinism, oculocutaneous
• MeSH C16.320.850.080.100.400 --- hermanski-pudlak syndrome
• MeSH C16.320.850.080.600 --- piebaldism
• MeSH C16.320.850.180 --- cutis laxa
• MeSH C16.320.850.210 --- dermatitis, atopic
• MeSH C16.320.850.235 --- dyskeratosis congenita
• MeSH C16.320.850.250 --- ectodermal dysplasia
• MeSH C16.320.850.250.398 --- ellis-van creveld syndrome
• MeSH C16.320.850.250.424 --- focal dermal hypoplasia
• MeSH C16.320.850.250.712 --- neurocutaneous syndromes
• MeSH C16.320.850.260 --- ehlers-danlos syndrome
• MeSH C16.320.850.275 --- epidermolysis bullosa
• MeSH C16.320.850.275.160 --- epidermolysis bullosa dystrophica
• MeSH C16.320.850.275.170 --- epidermolysis bullosa, junctional
• MeSH C16.320.850.275.180 --- epidermolysis bullosa simplex
• MeSH C16.320.850.400 --- ichthyosiform erythroderma, congenital
• MeSH C16.320.850.400.375 --- hyperkeratosis, epidermolytic
• MeSH C16.320.850.400.410 --- ichthyosis, lamellar
• MeSH C16.320.850.405 --- ichthyosis vulgaris
• MeSH C16.320.850.408 --- ichthyosis, x-linked
• MeSH C16.320.850.420 --- incontinentia pigmenti
• MeSH C16.320.850.475 --- keratoderma, palmoplantar
• MeSH C16.320.850.475.440 --- keratoderma, palmoplantar, diffuse
• MeSH C16.320.850.475.600 --- papillon-lefevre disease
• MeSH C16.320.850.490 --- keratosis follicularis
• MeSH C16.320.850.700 --- pemphigus, benign familial
• MeSH C16.320.850.730 --- porokeratosis
• MeSH C16.320.850.738 --- porphyria, erythropoietic
• MeSH C16.320.850.742 --- porphyrias, hepatic
• MeSH C16.320.850.742.074 --- coproporphyria, hereditary
• MeSH C16.320.850.742.150 --- porphyria, acute intermittent
• MeSH C16.320.850.742.250 --- porphyria cutanea tarda
• MeSH C16.320.850.742.437 --- porphyria, hepatoerythropoietic
• MeSH C16.320.850.742.625 --- porphyria, variegate
• MeSH C16.320.850.742.812 --- protoporphyria, erythropoietic
• MeSH C16.320.850.750 --- pseudoxanthoma elasticum
• MeSH C16.320.850.765 --- rothmund-thomson syndrome
• MeSH C16.320.850.820 --- sjogren-larsson syndrome
• MeSH C16.320.850.970 --- xeroderma pigmentosum

[edit] MeSH C16.320.925 --- werner syndrome

[edit] MeSH C16.614 --- infant, newborn, diseases

[edit] MeSH C16.614.042 --- amniotic band syndrome

[edit] MeSH C16.614.053 --- anemia, neonatal

• MeSH C16.614.053.344 --- fetofetal transfusion
• MeSH C16.614.053.511 --- fetomaternal transfusion

[edit] MeSH C16.614.092 --- asphyxia neonatorum

[edit] MeSH C16.614.131 --- birth injuries

• MeSH C16.614.131.587 --- paralysis, obstetric

[edit] MeSH C16.614.213 --- cystic fibrosis

[edit] MeSH C16.614.258 --- epilepsy, benign neonatal

[edit] MeSH C16.614.304 --- erythroblastosis, fetal

• MeSH C16.614.304.502 --- kernicterus

[edit] MeSH C16.614.378 --- hemorrhagic disease of newborn

[edit] MeSH C16.614.390 --- hernia, umbilical

[edit] MeSH C16.614.414 --- hydrocephalus

• MeSH C16.614.414.200 --- dandy-walker syndrome

[edit] MeSH C16.614.438 --- hydrophthalmos

[edit] MeSH C16.614.451 --- hyperbilirubinemia, neonatal

• MeSH C16.614.451.500 --- jaundice, neonatal
• MeSH C16.614.451.500.250 --- jaundice, chronic idiopathic

[edit] MeSH C16.614.465 --- hyperostosis, cortical, congenital

[edit] MeSH C16.614.492 --- ichthyosis

• MeSH C16.614.492.400 --- ichthyosiform erythroderma, congenital
• MeSH C16.614.492.400.375 --- hyperkeratosis, epidermolytic
• MeSH C16.614.492.400.410 --- ichthyosis, lamellar
• MeSH C16.614.492.420 --- ichthyosis, x-linked
• MeSH C16.614.492.723 --- sjogren-larsson syndrome

[edit] MeSH C16.614.521 --- infant, premature, diseases

• MeSH C16.614.521.125 --- bronchopulmonary dysplasia
• MeSH C16.614.521.450 --- leukomalacia, periventricular
• MeSH C16.614.521.563 --- respiratory distress syndrome, newborn
• MeSH C16.614.521.563.475 --- hyaline membrane disease
• MeSH C16.614.521.731 --- retinopathy of prematurity

[edit] MeSH C16.614.580 --- meconium aspiration syndrome

[edit] MeSH C16.614.595 --- mobius syndrome

[edit] MeSH C16.614.610 --- neonatal abstinence syndrome

[edit] MeSH C16.614.643 --- nystagmus, congenital

[edit] MeSH C16.614.677 --- ophthalmia neonatorum

[edit] MeSH C16.614.694 --- persistent fetal circulation syndrome

[edit] MeSH C16.614.716 --- persistent hyperinsulinemia hypoglycemia of infancy

[edit] MeSH C16.614.760 --- rothmund-thomson syndrome

[edit] MeSH C16.614.810 --- sclerema neonatorum

[edit] MeSH C16.614.815 --- severe combined immunodeficiency

[edit] MeSH C16.614.868 --- syphilis, congenital

[edit] MeSH C16.614.890 --- thanatophoric dysplasia

[edit] MeSH C16.614.909 --- toxoplasmosis, congenital

[edit] MeSH C16.614.947 --- wolman disease