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Disease Ontology Browser
hypotrichosis 11 (DOID:0110708)
Alliance: disease page
Synonyms: Hypt11
Alt IDs: OMIM:615059
Definition: A hypotrichosis that has_material_basis_in a autosomal dominant mutation of SNRPE on chromosome 1q32.1.


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
01/24/2023
MGI 6.22
The Jackson Laboratory