ODCs

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7 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Total congenital cataract

Familial hypocalciuric hypercalcemia type 3


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EPHA2	(0.63)	AP2S1

Citations in the biomedical literature:

Total congenital cataract		Familial hypocalciuric hypercalcemia type 3
	Synonym(s): (no synonyms)		Synonym(s): - FHH type 3

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

	External references: 7 OMIM references - 1 MeSH reference: C535341		External references: 1 OMIM reference - 1 MeSH reference: C537147

No signs/symptoms info available.