retinitis pigmentosa 38

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Summary

Literature (0)

DOID:0110367 - retinitis pigmentosa 38

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the MERTK gene on chromosome 2q13.

Synonyms: RP38

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: mertk

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013469 - retinitis pigmentosa 38

MONDO:0013469 - retinitis pigmentosa 38

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), retinitis pigmentosa (is_a)