congenital hypotrichosis with juvenile macular dystrophy Disease Ontology Browser

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congenital hypotrichosis with juvenile macular dystrophy (DOID:0110711)
Alliance: disease page
Synonyms: HJMD; hypotrichosis with cone-rod dystrophy
Alt IDs: OMIM:601553
Definition: A hypotrichosis that has_material_basis_in a autosomal recessive mutation of the CDH3 gene on chromosome 16q22.1.

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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