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Echinobase
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, HMSN IC, HMSN1C, Charcot-Marie-Tooth neuropathy type 1C, neuropathy hereditary motor and sensory type 1C

Echinobase Genes :


MIM:
MIM:601098 - charcot-marie-tooth disease, demyelinating, type 1c; cmt1c

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

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