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Disease Ontology Browser
X-linked recessive hypophosphatemic rickets (DOID:0080353)
Alliance: disease page
Alt IDs: OMIM:300554
Definition: A rickets that has_material_basis_in mutation in the CLCN5 gene on chromosome Xp11.22.


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
12/10/2024
MGI 6.24
The Jackson Laboratory