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Summary Literature (0)
DOID:0111025 - cone-rod dystrophy 19

Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the TTLL5 gene on chromosome 14q24.

Synonyms: CORD19,

Xenbase Genes : ttll5

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014372 - cone-rod dystrophy 19


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)