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Disease Ontology Browser
Charcot-Marie-Tooth disease type 1C (DOID:0110151)
Alliance: disease page
Synonyms: Charcot-Marie-Tooth neuropathy type 1C; CMT1C; CMT slow nerve conduction type C; HMSN1C; HMSN IC; neuropathy hereditary motor and sensory type 1C
Alt IDs: OMIM:601098, ICD10CM:G60.0, MESH:C537984, ORDO:101083
Definition: A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the LITAF gene on chromosome 16p13.

Disease References using Mouse Models (2)
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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12/17/2024
MGI 6.24 		The Jackson Laboratory