ZFIN Human Disease: retinitis pigmentosa 1

OBO ID: DOID:0110390

OBO ID: DOID:0110390

Term Name:	retinitis pigmentosa 1	Search Ontology:
Synonyms:	RP1
Definition:	A retinitis pigmentosa that has_material_basis_in mutation in the RP1 gene on chromosome 8q12. https://www.ncbi.nlm.nih.gov/pubmed/10391211
References:	ICD10CM:H35.5 MESH:C538365 OMIM:180100
Ontology:	Human Disease ( DOID:0110390 )

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 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
RP1	rp1	Retinitis pigmentosa 1	180100

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None