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Disease Ontology Browser
autosomal dominant woolly hair (DOID:0111573)
Alliance: disease page
Synonyms: ADWH
Alt IDs: OMIM:194300
Definition: A familial woolly hair syndrome that has_material_basis_in heterozygous mutation in the KRT74 gene on chromosome 12q13.13.


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
03/19/2024
MGI 6.23
The Jackson Laboratory