exudative vitreoretinopathy

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Information
Disease area statistics
Chromosome band
Annotation

Information

Disease name: exudative vitreoretinopathy
Disease ID: DOID:0050535
Description: "A retinal vascular disease characterized by the prevention of blood vessel formation at the edges of the retina and the hemorrhage of the blood vessels in the retina." [url:http\://en.wikipedia.org/wiki/Familial_exudative_vitreoretinopathy, url:http\://ghr.nlm.nih.gov/condition/familial-exudative-vitreoretinopathy]

Disease area statistics

Chromosome band

Gene symbol	Chromosome	Start	Stop	The number of variant
FZD4	11	86,945,679	86,955,395	40
PRSS23	11	86,800,542	86,811,233	32

Annotation

INFO

Disase is a (Disease Ontology): DOID:2462
Cross Reference ID (Disease Ontology): GARD:1613
Cross Reference ID (Disease Ontology): ICD10CM:H35.00
Cross Reference ID (Disease Ontology): ICD9CM:362.10
Cross Reference ID (Disease Ontology): MIM:PS133780
Cross Reference ID (Disease Ontology): ORDO:891
Cross Reference ID (Disease Ontology): SNOMEDCT_US_2023_03_01:193355009
Cross Reference ID (Disease Ontology): UMLS_CUI:C0004608
Exact Synonym (Disease Ontology): familial exudative vitreoretinopathy
Exact Synonym (Disease Ontology): FEVR
HPO Human Phenotype ID (Human Phenotype Ontology): HP:0030490
OMIM Phenotype Series Number (OMIM): PS133780
MedGen concept unique identifier (MedGen Concept name): C4072980
MedGen unique identifier (MedGen Concept name): 892913