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Coppock-like cataract

4 OMIM references -
4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Syndactyly type 3

1 OMIM reference -
1 associated gene
4 signs/symptoms

Coppock-like cataract

Syndactyly type 3

CRYBB2	(UniProt - OMIM)		GJA1	(UniProt - OMIM)
CRYGC	(UniProt - OMIM)
CRYGD	(UniProt - OMIM)
GJA3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GJA3	(0.73)	GJA1

Citations in the biomedical literature:

Coppock-like cataract		Syndactyly type 3
	Synonym(s): (no synonyms)		Synonym(s): - SD3 - Syndactyly of fingers 4 and 5

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C538154

Syndactyly type 3
	Very frequent - Autosomal dominant inheritance - Syndactyly of fingers / interdigital palm Frequent - Camptodactyly of some fingers Occasional - Short foot / brachydactyly of toes
Coppock-like cataract
(no data available)