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Disease Ontology Browser
autosomal recessive woolly hair 3 (DOID:0111574)
Alliance: disease page
Synonyms: ARWH3
Alt IDs: OMIM:616760
Definition: A familial woolly hair syndrome that has_material_basis_in homozygous or compound heterozygous mutation in KRT24 on chromosome 17q21.2.


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
09/27/2022
MGI 6.21
The Jackson Laboratory