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Disease Ontology Browser
Charcot-Marie-Tooth disease axonal type 2T (DOID:0110160)
Alliance: disease page
Synonyms: AR-CMT2T; autosomal recessive axonal Charcot-Marie-Tooth disease type 2T; Charcot-Marie-Tooth neuropathy type 2T; CMT2T
Alt IDs: OMIM:617017, ICD10CM:G60.0, ORDO:443950
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.


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
02/11/2020
MGI 6.14
The Jackson Laboratory