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GENE - TERM ANNOTATION REPORT

RGD ID: 1616754
Species: Mus musculus
RGD Object: Gene
Symbol: Cyp2c66
Name: cytochrome P450, family 2, subfamily c, polypeptide 66
Acc ID: DOID:9002088
Term: MITCHELL SYNDROME
Definition: A progressive disorder caused by heterozygous mutation in the ACOX1 gene and characterized by episodic demyelination, sensorimotor polyneuropathy, and hearing loss.
Definition Source(s): OMIM:618960
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
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