Search Ontology:
Human Disease
Mitchell syndrome
- Term ID
- DOID:0070516
- Synonyms
-
- 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. (2)
- References
-
- MIM:618960
- ORDO:631248
- UMLS_CUI:C5394554
- Ontology
- Human Disease ( DOID:0070516 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models