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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](img/icons/info1.png)
MIM:614500 - cone-rod dystrophy 16; cord16 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
cone-rod dystrophy (is_a)