cone-rod dystrophy 16

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Echinobase

Summary

Literature (0)

DOID:0111022 - cone-rod dystrophy 16

Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22.

Synonyms: CORD16, retinal dystrophy with early macular involvement

Echinobase 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

: c8orf37

MIM:

MIM:614500 - cone-rod dystrophy 16; cord16

MIM:614500 - cone-rod dystrophy 16; cord16

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)