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Coppock-like cataract
4 OMIM references -
4 associated genes
25 connected diseases
No signs/symptoms info
Disease Type of connection
Cataract-microcornea syndrome
Nuclear cataract
Zonular cataract
Cerulean cataract
Pulverulent cataract
Cataract with Y-shaped suture opacities
Total congenital cataract
Posterior polar cataract
Coralliform cataract
Alpha-crystallinopathy
Familial isolated dilated cardiomyopathy
Fatal infantile hypertonic myofibrillar myopathy
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Distal hereditary motor neuropathy type 2
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Craniometaphyseal dysplasia
Hypoplastic left heart syndrome
Oculodentodigital dysplasia
Syndactyly type 3
Microphthalmia - cataract
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Spinocerebellar ataxia type 14
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
4 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
CRYBB2 P43320123620
CRYGC P07315123680
CRYGD P07320123690
GJA3 Q9Y6H8121015
No signs/symptoms info available.