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Disease Ontology Browser
Charcot-Marie-Tooth disease type 1C (DOID:0110151)
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, 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 (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/12/2017
MGI 6.10
The Jackson Laboratory