ODCs

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2 associated genes
No signs/symptoms info

COMMON GENES: 1

2 OMIM references -
3 associated genes
No signs/symptoms info

Congenital cataract microcornea with corneal opacity

Persistent hyperplastic primary vitreous

Citations in the biomedical literature:

Congenital cataract microcornea with corneal opacity		Persistent hyperplastic primary vitreous
	Synonym(s): - CCMCO		Synonym(s): - PFVS - PHPV - Persistent fetal vasculature syndrome

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 2 OMIM references - 1 MeSH reference: D054514

No signs/symptoms info available.