ODCs

Click node...

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

COMMON GENES: 2
PROTEIN INTERACTIONS: 2

1 OMIM reference -
3 associated genes
No signs/symptoms info

Persistent hyperplastic primary vitreous

Retinopathy of prematurity


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FZD4 NDP	(0.84) (0.63)	NDP LRP5

Citations in the biomedical literature:

Persistent hyperplastic primary vitreous		Retinopathy of prematurity
	Synonym(s): - PFVS - PHPV - Persistent fetal vasculature syndrome		Synonym(s): - ROP - Retrolental fibroplasia

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the eye and adnexa -

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

	External references: 2 OMIM references - 1 MeSH reference: D054514		External references: 1 OMIM reference - 1 MeSH reference: D012178

No signs/symptoms info available.