List of MeSH codes (C16)
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".)
MeSH C16 --- congenital, hereditary, and neonatal diseases and abnormalities
MeSH C16.131 --- abnormalities
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
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
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
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
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
MeSH C16.131.482 --- lymphatic abnormalities
- MeSH C16.131.482.500 --- lymphangiectasis, intestinal
MeSH C16.131.581 --- monsters
- MeSH C16.131.581.197 --- anencephaly
- MeSH C16.131.581.806 --- twins, conjoined
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
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
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
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
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
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
MeSH C16.131.894 --- thyroid dysgenesis
- MeSH C16.131.894.500 --- lingual thyroid
- MeSH C16.131.894.500.500 --- lingual goiter
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
MeSH C16.300 --- fetal diseases
MeSH C16.300.060 --- erythroblastosis, fetal
MeSH C16.320 --- genetic diseases, inborn
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
MeSH C16.320.077 --- anemia, hypoplastic, congenital
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
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
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
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
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
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
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
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 --- Hereditary 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
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
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
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
MeSH C16.614 --- infant, newborn, diseases
MeSH C16.614.053 --- anemia, neonatal
- MeSH C16.614.053.344 --- fetofetal transfusion
- MeSH C16.614.053.511 --- fetomaternal transfusion
MeSH C16.614.131 --- birth injuries
- MeSH C16.614.131.587 --- paralysis, obstetric
MeSH C16.614.304 --- erythroblastosis, fetal
MeSH C16.614.414 --- hydrocephalus
MeSH C16.614.451 --- hyperbilirubinemia, neonatal
- MeSH C16.614.451.500 --- jaundice, neonatal
- MeSH C16.614.451.500.250 --- jaundice, chronic idiopathic
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
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
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