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Disease Ontology Browser
X-linked retinal dystrophy, Gardner-Hardcastle type (DOID:0070828)
Alliance: disease page
Synonyms: RDXGH
Alt IDs: OMIM:301149, UMLS_CUI:C6012691
Definition: A retinal degeneration characterized by early childhood onset of night blindness or light sensitivity, reduced visual acuity, and variable maculopathy with foveal hypoplasia that has_material_basis_in hemizygous interchromosomal insertion at chromosome Xq27.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
09/01/2026
MGI 6.24 		The Jackson Laboratory