Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/3
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- Chromosome 1 ring
- 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, monosomy 10p
- Chromosome 10, monosomy 10q
- Chromosome 10, trisomy 10p
- Chromosome 10, trisomy 10pter p13
- Chromosome 10, uniparental disomy of
- Chromosome 10p terminal deletion syndrome
- Chromosome 11, partial trisomy 11q
- Chromosome 11-14 translocation
- 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 trisomy
- Chromosome 13q-mosaicism
- 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, trisomy mosaicism
- Chromosome 15q, tetrasomy
- 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 17q22
- Chromosome 18 long arm deletion syndrome
- Chromosome 18 mosaic monosomy
- Chromosome 18, deletion 18q23
- Chromosome 19 ring
- Chromosome 19, trisomy 19q
- Chromosome 1q, duplication 1q12 q21
- Chromosome 2, monosomy 2p22
- Chromosome 2, monosomy 2pter p24
- Chromosome 2, monosomy 2q24
- Chromosome 2, trisomy 2p
- Chromosome 2, Trisomy 2p13 p21
- Chromosome 2, trisomy 2pter p24
- Chromosome 2, trisomy 2q
- 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, monosome mosaic
- Chromosome 22, trisomy q11 q13
- Chromosome 3 duplication syndrome
- 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, 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 9 inversion or duplication
- Chromosome 9 Ring
- Chromosome 9, duplication 9q21
- Chromosomes 1 and 2, monosomy 2q duplication 1p
- Chudley Rozdilsky syndrome
- Ciliary discoordination, due to random ciliary orientation
- Ciliary dyskinesia, due to transposition of ciliary microtubules
- Circumscribed cutaneous aplasia of the vertex
- Clayton Smith Donnai syndrome
- Cleft lip and palate malrotation cardiopathy
- 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 pituitary deficiency
- Cleft lower lip cleft lateral canthi chorioretinal
- Cleft palate cardiac defect ectrodactyly
- Cleft palate heart disease polydactyly absent tibia
- Cleft palate stapes fixation oligodontia
- Cleft tongue syndrome
- Clefting ectropion conical teeth
- Cloverleaf skull micromelia thoracic dysplasia
- Coarse face hypotonia constipation
- Cohen Lockood Wyborney syndrome
- Colavita Kozlowski syndrome
- Coleman Randall syndrome
- Collins Sakati syndrome
- Coloboma porencephaly hydronephrosis
- Coloboma uveal with cleft lip palate and mental retardation
- Colobomatous microphthalmia
- Colver Steer Godman syndrome
- Complex 3 mitochondrial respiratory chain deficiency
- Complex 4 mitochondrial respiratory chain deficiency
- Complex 5 mitochondrial respiratory chain deficiency
- Conductive deafness malformed external ear
- Congenital aneurysms of the great vessels
- Congenital articular rigidity
- Congenital brain disorder
- Congenital craniosynostosis maternal hyperthyroiditis
- Congenital cystic eye multiple ocular and intracranial anomalies
- Congenital gastrointestinal disorder
- Congenital heart disease ptosis hypodontia craniostosis
- Congenital heart disease radio ulnar synostosis mental retardation
- Congenital hypomyelination neuropathy
- Congenital hypotrichosis milia
- Congenital ichthyosis, microcephalus, quadriplegia
- Congenital kidney disorder
- Congenital mitral malformation
- Congenital mixovirus
- Congenital muscular dystrophy syringomyelia
- Congenital short femur
- Congenital skin disorder
- Congenital unilateral pulmonary hypoplasia
- Congenital vagal hyperreflexivity
- Conjunctivitis with Pseudomembrane
- Conotruncal heart malformations
- Continuous spike-wave during slow sleep syndrome
- Contractures ectodermal dysplasia cleft lip palate
- Contractures hyperkeratosis lethal
- Corneal crystals myopathy neuropathy
- Corneal dystrophy epithelial short stature
- Corneal dystrophy ichthyosis microcephaly mental retardation
- Corneal dystrophy pigmentary anomaly malabsorption
- Coronal synostosis syndactyly jejunal atresia
- Coronaro-cardiac fistula
- Coronary arteries congenital malformation
- Corpus callosum agenesis double urinary collecting
- Corpus callosum dysgenesis cleft spasm
- Corsello Opitz syndrome
- Cortada Koussef Matsumoto syndrome
- Cortical blindness mental retardation polydactyly
- Cortical degeneration of the cerebellum parenchymatous
- Costocoracoid ligament congenitally short
- Cote Katsantoni syndrome
- Coxoauricular syndrome
- Cranioacrofacial syndrome
- Craniofacial deafness hand syndrome
- Craniofacial dysostosis arthrogryposis progeroid appearance
- Craniofaciocervical osteoglyphic dysplasia
- Craniomicromelic syndrome
- Craniostenosis cataract
- Craniosynostosis arthrogryposis cleft palate
- Craniosynostosis cleft lip palate arthrogryposis
- Craniosynostosis contractures cleft
- Craniosynostosis exostoses nevus epibulbar dermoid
- Craniosynostosis fibular aplasia
- Craniosynostosis mental retardation clefting syndrome
- Craniosynostosis synostoses hypertensive nephropathy
- Craniotelencephalic dysplasia
- Crawfurd syndrome
- Criss cross syndrome
- Crossed polydactyly type 1
- Cryptomicrotia brachydactyly syndrome excess fingers
- Cryptomicrotia brachydactyly syndrome
- Culler Jones syndrome
- Curry Hall syndrome
- Curtis Rogers Stevenson syndrome
- Cutaneous photosensitivity colitis lethal
- Cutis verticis gyrata thyroid aplasia mental retardation
- Cutler Bass Romshe syndrome
- Cystic angiomatosis of bone, diffuse
- Cytoplasmic body myopathy
- Czeizel Losonci syndrome