ZFIN Human Disease: retinitis pigmentosa 4

OBO ID: DOID:0110372

Term Name:	retinitis pigmentosa 4		Search Ontology:
Synonyms:	RP4
Definition:	A retinitis pigmentosa that has_material_basis_in mutation in the RHO gene on chromosome 3q22. https://www.ncbi.nlm.nih.gov/pubmed/2137202
References:	ICD10CM:H35.5 MESH:C566706 OMIM:613731
Ontology:	Human Disease ( DOID:0110372 )

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 4 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
RHO	rho	Retinitis pigmentosa 4, autosomal dominant or recessive	613731

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None