ZFIN Human Disease: retinitis pigmentosa 37

OBO ID: DOID:0110399

Term Name:	retinitis pigmentosa 37		Search Ontology:
Synonyms:	RP37
Definition:	A retinitis pigmentosa that has_material_basis_in mutation in the NR2E3 gene on chromosome 15q23. https://www.ncbi.nlm.nih.gov/pubmed/17564971
References:	ICD10CM:H35.5 MESH:C567005 OMIM:611131
Ontology:	Human Disease ( DOID:0110399 )

Relationships

is a type of:	autosomal dominant disease autosomal recessive disease retinitis pigmentosa autosomal dominant disease autosomal recessive disease retinitis pigmentosa Show first 5 Terms

OTHER retinitis pigmentosa 37 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NR2E3	nr2e3	Retinitis pigmentosa 37	611131

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None