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Summary Literature (0)
DOID:0110151 - Charcot-Marie-Tooth disease type 1C

Disease Ontology Definition:A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the LITAF gene on chromosome 16p13.

Synonyms: CMT slow nerve conduction type C, CMT1C, Charcot-Marie-Tooth neuropathy type 1C, HMSN IC, HMSN1C, neuropathy hereditary motor and sensory type 1C,

Xenbase Genes : litaf

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010995 - Charcot-Marie-Tooth disease type 1C


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Charcot-Marie-Tooth disease type 1 (is_a), autosomal dominant disease (is_a)