cone-rod dystrophy 20

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Summary

Literature (0)

DOID:0111026 - cone-rod dystrophy 20

Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the POC1B gene on chromosome 12q21.

Synonyms: CORD20

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

: poc1b

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014427 - cone-rod dystrophy 20

MONDO:0014427 - cone-rod dystrophy 20

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

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

Parent(s): cone-rod dystrophy (is_a)