Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/3
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- Chromosomal triplication
- Chromosome 1 ring
- Chromosome 1, 1p36 deletion syndrome
- Chromosome 1, deletion q21 q25
- Chromosome 1, duplication 1p21 p32
- Chromosome 1, monosomy 1p
- Chromosome 1, monosomy 1p22 p13
- Chromosome 1, monosomy 1p31 p22
- Chromosome 1, monosomy 1p32
- Chromosome 1, monosomy 1p34 p32
- Chromosome 1, monosomy 1q25 q32
- Chromosome 1, monosomy 1q32 q42
- Chromosome 1, monosomy 1q4
- Chromosome 1, q42 11 q42 12 duplication
- Chromosome 1, trisomy 1q32 qter
- Chromosome 1, trisomy 1q42 qter
- Chromosome 1, uniparental disomy 1q12 q21
- Chromosome 10 ring
- Chromosome 10, distal trisomy 10q
- Chromosome 10, monosomy 10p
- Chromosome 10, monosomy 10q
- Chromosome 10, trisomy 10p
- Chromosome 10, trisomy 10pter p13
- Chromosome 10, trisomy 10q
- Chromosome 10, uniparental disomy of
- Chromosome 10p terminal deletion syndrome
- Chromosome 11, deletion 11p
- Chromosome 11, partial trisomy 11q
- Chromosome 11-14 translocation
- Chromosome 11p, partial deletion
- Chromosome 11q partial deletion
- Chromosome 11q trisomy
- Chromosome 12 ring
- Chromosome 12, 12p trisomy
- Chromosome 12, trisomy 12q
- Chromosome 12p deletion
- Chromosome 12p partial deletion
- Chromosome 13 duplication
- Chromosome 13 ring
- Chromosome 13, partial monosomy 13q
- Chromosome 13p duplication
- Chromosome 13q deletion
- Chromosome 13q trisomy
- Chromosome 13q-mosaicism
- Chromosome 14 ring
- Chromosome 14 trisomy
- Chromosome 14, deletion 14q, partial duplication 14p
- Chromosome 14, trisomy mosaic
- Chromosome 14q, partial deletions
- Chromosome 14q, proximal duplication
- Chromosome 14q, terminal deletion
- Chromosome 14q, terminal duplication
- Chromosome 15 ring
- Chromosome 15, distal trisomy 15q
- Chromosome 15, trisomy mosaicism
- Chromosome 15q, tetrasomy
- Chromosome 16, trisomy 16p
- Chromosome 16, trisomy 16q
- Chromosome 16, trisomy
- Chromosome 16, uniparental disomy
- Chromosome 17 deletion
- Chromosome 17 ring
- Chromosome 17 trisomy
- Chromosome 17, deletion 17q23 q24
- Chromosome 17, trisomy 17p
- Chromosome 17, trisomy 17p11 2
- Chromosome 17, trisomy 17q22
- Chromosome 18 long arm deletion syndrome
- Chromosome 18 mosaic monosomy
- Chromosome 18 ring
- Chromosome 18, deletion 18q23
- Chromosome 18, monosomy 18p
- Chromosome 18, tetrasomy 18p
- Chromosome 18, trisomy 18p
- Chromosome 18, trisomy 18q
- Chromosome 18, trisomy
- Chromosome 19 ring
- Chromosome 19, trisomy 19q
- Chromosome 1q, duplication 1q12 q21
- Chromosome 2, monosomy 2p22
- Chromosome 2, monosomy 2pter p24
- Chromosome 2, monosomy 2q
- Chromosome 2, monosomy 2q24
- Chromosome 2, monosomy 2q37
- Chromosome 2, trisomy 2p
- Chromosome 2, Trisomy 2p13 p21
- Chromosome 2, trisomy 2pter p24
- Chromosome 2, trisomy 2q
- Chromosome 2, trisomy 2q37
- Chromosome 20 ring
- Chromosome 20, deletion 20p
- Chromosome 20, duplication 20p
- Chromosome 20, trisomy
- Chromosome 21 monosomy
- Chromosome 21 ring
- Chromosome 21, monosomy 21q22
- Chromosome 21, tetrasomy 21q
- Chromosome 21, uniparental disomy of
- Chromosome 22 ring
- Chromosome 22 trisomy mosaic
- Chromosome 22, monosome mosaic
- Chromosome 22, trisomy q11 q13
- Chromosome 22, trisomy
- Chromosome 3 duplication syndrome
- Chromosome 3, monosomy 3p
- Chromosome 3, monosomy 3p14 p11
- Chromosome 3, monosomy 3p2
- Chromosome 3, monosomy 3p25
- Chromosome 3, monosomy 3q13
- Chromosome 3, monosomy 3q21 23
- Chromosome 3, monosomy 3q27
- Chromosome 3, trisomy 3p
- Chromosome 3, trisomy 3p25
- Chromosome 3, trisomy 3q
- Chromosome 3, trisomy 3q13 2 q25
- Chromosome 3, Trisomy 3q2
- Chromosome 4 ring
- Chromosome 4 short arm deletion
- Chromosome 4, monosomy 4p14 p16
- Chromosome 4, monosomy 4q
- Chromosome 4, monosomy 4q32
- Chromosome 4, monosomy distal 4q
- Chromosome 4, partial trisomy distal 4q
- Chromosome 4, Trisomy 4p
- Chromosome 4, trisomy 4q
- Chromosome 4, trisomy 4q21
- Chromosome 4, trisomy 4q25 qter
- Chromosome 5, monosomy 5q35
- Chromosome 5, trisomy 5p
- Chromosome 5, trisomy 5pter p13 3
- Chromosome 5, trisomy 5q
- Chromosome 5, uniparental disomy
- Chromosome 6 ring
- Chromosome 6, deletion 6q13 q15
- Chromosome 6, monosomy 6p23
- Chromosome 6, monosomy 6q
- Chromosome 6, monosomy 6q1
- Chromosome 6, monosomy 6q2
- Chromosome 6, partial trisomy 6q
- Chromosome 6, trisomy 6p
- Chromosome 6, trisomy 6q
- Chromosome 7 ring
- Chromosome 7, monosomy 7q2
- Chromosome 7, monosomy 7q21
- Chromosome 7, monosomy 7q3
- Chromosome 7, monosomy
- Chromosome 7, partial monosomy 7p
- Chromosome 7, trisomy 7p
- Chromosome 7, trisomy 7p13 p12 2
- Chromosome 7, trisomy 7q
- Chromosome 7, trisomy mosaic
- Chromosome 8 deletion
- Chromosome 8 ring
- Chromosome 8, monosomy 8p
- Chromosome 8, monosomy 8p2
- Chromosome 8, monosomy 8p23 1
- Chromosome 8, monosomy 8q
- Chromosome 8, mosaic trisomy
- Chromosome 8, partial trisomy
- Chromosome 8, trisomy 8p
- Chromosome 8, trisomy 8q
- Chromosome 8, trisomy
- Chromosome 9 inversion or duplication
- Chromosome 9 Ring
- Chromosome 9, duplication 9q21
- Chromosome 9, monosomy 9p
- Chromosome 9, partial monosomy 9p
- Chromosome 9, partial trisomy 9p
- Chromosome 9, tetrasomy 9p
- Chromosome 9, trisomy 9q
- Chromosome 9, trisomy 9q32
- Chromosome 9, trisomy mosaic
- Chromosome 9, trisomy
- Chromosomes 1 and 2, monosomy 2q duplication 1p
- Chronic berylliosis
- Chronic demyelinizing neuropathy with IgM monoclonal
- Chronic erosive gastritis
- Chronic myelomonocytic leukemia
- Chronic necrotizing vasculitis
- Chronic neutropenia
- Chronic polyradiculoneuritis
- Chronic recurrent multifocal osteomyelitis
- Chronic, infantile, neurological, cutaneous, articular syndrome
- Chudley Lowry Hoar syndrome
- Chudley Rozdilsky syndrome
- Chudley-Mccullough syndrome
- Chylous ascites
- Cicatricial pemphigoid
- Ciliary discoordination, due to random ciliary orientation
- Ciliary dyskinesia, due to transposition of ciliary microtubules
- Ciliary dyskinesia-bronchiectasis
- Cilliers Beighton syndrome
- Circumscribed cutaneous aplasia of the vertex
- Circumscribed disseminated keratosis Jadassohn Lew type
- Clarkson disease
- Clayton Smith Donnai syndrome
- Cleft hand absent tibia
- Cleft lip and palate malrotation cardiopathy
- Cleft lip and/or palate with mucous cysts of lower
- Cleft lip palate abnormal thumbs microcephaly
- Cleft lip palate deafness sacral lipoma
- Cleft lip palate dysmorphism Kumar type
- Cleft lip palate ectrodactyly
- Cleft lip palate incisor and finger anomalies
- Cleft lip palate mental retardation corneal opacity
- Cleft lip palate oligodontia syndactyly pili torti
- Cleft lip palate pituitary deficiency
- Cleft lip palate-tetraphocomelia
- Cleft lip with or without cleft palate
- Cleft lower lip cleft lateral canthi chorioretinal
- Cleft palate cardiac defect ectrodactyly
- Cleft palate colobomata radial synostosis deafness
- Cleft palate heart disease polydactyly absent tibia
- Cleft palate lateral synechia syndrome
- Cleft palate short stature vertebral anomalies
- Cleft palate stapes fixation oligodontia
- Cleft palate X linked
- Cleft tongue syndrome
- Cleft upper lip median cutaneous polyps
- Clefting ectropion conical teeth
- Cleidocranial dysplasia micrognathia absent thumbs
- Cleisiophobia
- Clouston syndrome
- Cloverleaf skull bone dysplasia
- Cloverleaf skull micromelia thoracic dysplasia]]
- Coach syndrome
- Coal worker's pneumoconiosis
- Coarctation of aorta dominant
- Coarse face hypotonia constipation
- Cocaine antenatal infection
- Cocaine fetopathy
- Cochin Jewish Disorder
- Cockayne syndrome type 1
- Cockayne syndrome type 2
- Cockayne syndrome type 3
- Codas syndrome
- Coenzyme Q cytochrome c reductase deficiency of
- Coffin-Siris syndrome
- COFS syndrome
- Cogan-Reese syndrome
- Cohen Hayden syndrome
- Cohen Lockood Wyborney syndrome
- Colavita Kozlowski syndrome
- Cold agglutination syndrome
- Cold agglutinin disease
- Cold antibody hemolytic anemia
- Cole carpenter syndrome
- Coleman Randall syndrome
- Collagen disorder
- Collins Pope syndrome
- Collins Sakati syndrome
- Coloboma chorioretinal cerebellar vermis aplasia
- Coloboma hair abnormality
- Coloboma of choroid and retina
- Coloboma of lens ala nasi
- Coloboma of macula type B brachydactyly
- Coloboma porencephaly hydronephrosis
- Coloboma uveal with cleft lip palate and mental retardation
- Colobomata unilobar lung heart defect
- Colobomatous microphthalmia heart disease hearing
- Colobomatous microphthalmia
- Colon cancer, familial nonpolyposis
- Colonic atresia
- Colonic malakoplakia
- Colver Steer Godman syndrome
- Combarros Calleja Leno syndrome
- Common mesentery
- Complement component 2 deficiency
- Complement component receptor 1
- Complete atrioventricular canal
- Complex 1 mitochondrial respiratory chain deficiency
- Complex 2 mitochondrial respiratory chain deficiency
- Complex 3 mitochondrial respiratory chain deficiency
- Complex 4 mitochondrial respiratory chain deficiency
- Complex 5 mitochondrial respiratory chain deficiency
- Conductive deafness malformed external ear
- Cone rod dystrophy amelogenesis imperfecta
- Cone rod dystrophy
- Congenital absence of the uterus and vagina
- Congenital alopecia X linked
- Congenital amputation
- Congenital aneurysms of the great vessels
- Congenital aplastic anemia
- Congenital arteriovenous shunt
- Congenital articular rigidity
- Congenital benign spinal muscular atrophy dominant
- Congenital brain disorder
- Congenital bronchobiliary fistula
- Congenital cardiovascular disorder
- Congenital cardiovascular malformations
- Congenital cardiovascular shunt
- Congenital constricting band
- Congenital contractual arachnodactyly
- Congenital contractures
- Congenital craniosynostosis maternal hyperthyroiditis
- Congenital cystic eye multiple ocular and intracranial anomalies
- Congenital cytomegalovirus
- Congenital fiber type disproportion
- Congenital gastrointestinal disorder
- Congenital generalized fibromatosis
- Congenital giant megaureter
- Congenital heart block
- Congenital heart disease ptosis hypodontia craniostosis
- Congenital heart disease radio ulnar synostosis mental retardation
- Congenital hemidysplasia with ichtyosiform erythroderma and limbs defects
- Congenital hemolytic anemia
- Congenital hepatic fibrosis
- Congenital hepatic porphyria
- Congenital hypomyelination neuropathy
- Congenital hypotrichosis milia
- Congenital ichthyosis, microcephalus, quadriplegia
- Congenital ichtyosiform erythroderma
- Congenital kidney disorder
- Congenital lobar emphysema
- Congenital megacolon
- Congenital megalo-ureter
- Congenital mesoblastic nephroma
- Congenital microvillous atrophy
- Congenital mitral malformation
- Congenital mitral stenosis
- Congenital mixovirus
- Congenital muscular dystrophy syringomyelia
- Congenital myopathy
- Congenital nephrotic syndrome, Finnish type
- Congenital nonhemolytic jaundice
- Congenital short bowel
- Congenital short femur
- Congenital skeletal disorder
- Congenital skin disorder
- Congenital spherocytic anemia
- Congenital spherocytic hemolytic anemia
- Congenital stenosis of cervical medullary canal
- Congenital sucrose isomaltose malabsorption
- Congenital unilateral pulmonary hypoplasia
- Congenital vagal hyperreflexivity
- Congenital varicella syndrome
- Conjunctivitis ligneous
- Conjunctivitis with Pseudomembrane
- Connective tissue dysplasia Spellacy type
- Connexin 26 anomaly
- Conotruncal heart malformations
- Conradi-Hünermann syndrome
- Constrictive bronchiolitis
- Continuous muscle fiber activity hereditary
- Continuous spike-wave during slow sleep syndrome
- Contractural arachnodactyly
- Contractures ectodermal dysplasia cleft lip palate
- Contractures hyperkeratosis lethal
- Contractures of feet-muscle atrophy-oculomotor apraxia
- Convulsions benign familial neonatal dominant form
- Convulsions benign familial neonatal
- Cooks syndrome
- Copper deficiency familial benign
- Coprastasophobia
- Cormier Rustin Munnich syndrome
- Corneal anesthesia deafness mental retardation
- Corneal cerebellar syndrome
- Corneal crystals myopathy neuropathy
- Corneal dystrophy epithelial short stature
- Corneal dystrophy ichthyosis microcephaly mental retardation
- Corneal dystrophy perceptive deafness
- Corneal dystrophy pigmentary anomaly malabsorption
- Corneal endothelium dystrophy
- Corneodermatoosseous syndrome
- Coronal synostosis syndactyly jejunal atresia
- Coronaro-cardiac fistula
- Coronary arteries congenital malformation
- Coronary artery aneurysm
- Corpus callosum agenesis double urinary collecting
- Corpus callosum agenesis neuronopathy
- Corpus callosum agenesis of blepharophimosis Robin type
- Corpus callosum agenesis of with chorioretinal abnormalities
- Corpus callosum agenesis polysyndactyly
- Corpus callosum agenesis
- Corpus callosum dysgenesis cleft spasm
- Corpus callosum dysgenesis hypopituitarism
- Corpus callosum dysgenesis X linked recessive
- Corsello Opitz syndrome
- Cortada Koussef Matsumoto syndrome
- Cortes Lacassie syndrome
- Cortical blindness mental retardation polydactyly
- Cortical degeneration of the cerebellum parenchymatous
- Cortical hyperostosis syndactyly
- Costocoracoid ligament congenitally short
- Cote Adamopoulos Pantelakis syndrome
- Cote Katsantoni syndrome
- Cousin Walbraum Cegarra syndrome
- Covesdem syndrome
- Cowchock Wapner Kurtz syndrome
- Cowden's disease
- Coxoauricular syndrome
- Cramer Niederdellmann syndrome
- Cramp-fasciculations syndrome
- Crandall syndrome
- Crane-Heise syndrome
- Cranio osteoarthropathy
- Cranioacrofacial syndrome
- Craniodigital syndrome mental retardation
- Cranioectodermal dysplasia
- Craniofacial and osseous defects mental retardation
- Craniofacial and skeletal defects
- Craniofacial deafness hand syndrome
- Craniofacial dysostosis arthrogryposis progeroid appearance
- Craniofacial dysynostosis
- Craniofaciocardioskeletal syndrome
- Craniofaciocervical osteoglyphic dysplasia
- Craniofrontonasal dysplasia
- Craniofrontonasal syndrome Teebi type
- Craniometaphyseal dysplasia dominant type
- Craniometaphyseal dysplasia recessive type
- Craniomicromelic syndrome
- Craniostenosis cataract
- Craniostenosis with congenital heart disease mental retardation
- Craniosynostosis alopecia brain defect
- Craniosynostosis arthrogryposis cleft palate
- Craniosynostosis autosomal dominant
- Craniosynostosis cleft lip palate arthrogryposis
- Craniosynostosis contractures cleft
- Craniosynostosis exostoses nevus epibulbar dermoid
- Craniosynostosis fibular aplasia
- Craniosynostosis Fontaine type
- Craniosynostosis Maroteaux Fonfria type
- Craniosynostosis mental retardation clefting syndrome
- Craniosynostosis mental retardation heart defects
- Craniosynostosis Philadelphia type
- Craniosynostosis radial aplasia syndrome
- Craniosynostosis synostoses hypertensive nephropathy
- Craniosynostosis Warman type
- Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus
- Craniotelencephalic dysplasia
- Crawfurd syndrome
- Creatine deficiency
- Creeping disease
- Cretinism athyreotic
- Crigler Najjar syndrome type I
- Crisponi syndrome
- Criss cross syndrome
- Criswick-Schepens syndrome
- Crohn's disease of the esophagus
- Crome syndrome
- Cronkhite-Canada disease
- Crossed polydactyly type 1
- Crossed polysyndactyly
- Cryptogenic organized pneumopathy
- Cryptomicrotia brachydactyly syndrome excess fingers
- Cryptomicrotia brachydactyly syndrome
- Cryptophthalmos-syndactyly syndrome
- Cryptorchidism arachnodactyly mental retardation
- Crystal deposit disease
- Culler Jones syndrome
- Curly hair ankyloblepharon nail dysplasia syndrome
- Currarino triad
- Curry Hall syndrome
- Curth-Macklin type ichthyosis hystrix
- Curtis Rogers Stevenson syndrome
- Cushing syndrome, familial
- Cushing's symphalangism
- Cutaneous photosensitivity colitis lethal
- Cutaneous T-cell lymphoma
- Cutaneous vascularitis
- Cutis Gyrata syndrome of Beare and Stevenson
- Cutis gyratum acanthosis nigricans craniosynostosis
- Cutis laxa corneal clouding mental retardation
- Cutis laxa osteoporosis
- Cutis laxa with joint laxity and retarded development
- Cutis laxa, dominant type
- Cutis laxa, recessive type 1
- Cutis laxa, recessive type 2
- Cutis laxa, recessive
- Cutis marmorata telangiectatica congenita
- Cutis verticis gyrata mental deficiency
- Cutis verticis gyrata thyroid aplasia mental retardation
- Cutler Bass Romshe syndrome
- Cyclosporosis
- Cypress facial neuromusculoskeletal syndrome
- Cystathionine beta synthetase deficiency
- Cystic adenomatoid malformation of lung
- Cystic angiomatosis of bone, diffuse
- Cystic fibrosis gastritis megaloblastic anemia
- Cystic hamartoma of lung and kidney
- Cystic hygroma lethal cleft palate
- Cystic medial necrosis of aorta
- Cystin transport, protein defect of
- Cystinuria-lysinuria
- Cytochrome C oxidase deficiency
- Cytomegalic inclusion disease
- Cytoplasmic body myopathy
- Czeizel Losonci syndrome
- Czeizel syndrome
