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Disease Ontology Browser
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 CDH3 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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last database update
11/10/2020
MGI 6.16
The Jackson Laboratory