ZFIN Human Disease: retinitis pigmentosa 35

OBO ID: DOID:0110357

Term Name:	retinitis pigmentosa 35		Search Ontology:
Synonyms:	RP35
Definition:	A retinitis pigmentosa that has_material_basis_in mutation in the SEMA4A gene on chromosome 1q22. https://www.ncbi.nlm.nih.gov/pubmed/16199541
References:	ICD10CM:H35.5 MESH:C565206 OMIM:610282
Ontology:	Human Disease ( DOID:0110357 )

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 35 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SEMA4A	sema4ab sema4aa	Retinitis pigmentosa 35	610282

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None