Mitchell syndrome Disease Ontology Browser

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Disease Ontology Browser

Mitchell syndrome (DOID:0070516)
Alliance: disease page
Alt IDs: OMIM:618960, ORDO:631248, UMLS_CUI:C5394554
Definition: A peroxisomal disease characterized by progressive episodic demyelination, sensorimotor polyneuropathy, and hearing loss that has_material_basis_in heterozygous mutation in the ACOX1 gene on chromosome 17q25.1.

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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