ZFIN Human Disease: posterior polymorphous corneal dystrophy 1

OBO ID: DOID:0110855

Term Name:	posterior polymorphous corneal dystrophy 1		Search Ontology:
Synonyms:	Ched1 Corneal Endothelial Dystrophy 1, Autosomal Dominant Maumenee Corneal Dystrophy Ppcd1
Definition:	A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23. https://www.ncbi.nlm.nih.gov/pubmed/26749309
References:	ICD10CM:H18.50 OMIM:122000
Ontology:	Human Disease ( DOID:0110855 )

Relationships

is a type of:	autosomal dominant disease posterior polymorphous corneal dystrophy autosomal dominant disease posterior polymorphous corneal dystrophy Show first 5 Terms

OTHER posterior polymorphous corneal dystrophy 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
OVOL2		Corneal dystrophy, posterior polymorphous, 1

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None