ODCs

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

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
9 signs/symptoms

Persistent hyperplastic primary vitreous

Coats disease


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

Citations in the biomedical literature:

Persistent hyperplastic primary vitreous		Coats disease
	Synonym(s): - PFVS - PHPV - Persistent fetal vasculature syndrome		Synonym(s): - Congenital retinal telangiectasia - Leber miliary aneurysm

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic 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: Class of prevalence: unknown Average age onset: childhood Average age of death: normal Type of inheritance: sporadic

	External references: 2 OMIM references - 1 MeSH reference: D054514		External references: 1 OMIM reference - 1 MeSH reference: D058456

Coats disease
	Very frequent - Retinal vascular anomalies / retinal telangiectasia - Strabismus / squint Frequent - Glaucoma - Macular dystrophy / absence / hypoplasia of the macula - Retinal detachment Occasional - Aniridia / iris hypoplasia - Anterior chamber anomaly - Cataract / lens opacification - Visual loss / blindness / amblyopia
Persistent hyperplastic primary vitreous
(no data available)