OBO ID: DOID:0110151
Term Name: Charcot-Marie-Tooth disease type 1C Search Ontology:
Synonyms:
  • Charcot-Marie-Tooth neuropathy type 1C
  • CMT slow nerve conduction type C
  • CMT1C
  • HMSN IC
  • HMSN1C
  • neuropathy hereditary motor and sensory type 1C
Definition: A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the LITAF gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/12525712
References:
Ontology: Human Disease   ( DOID:0110151 )
Relationships
is a type of:
OTHER Charcot-Marie-Tooth disease type 1C PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LITAF Charcot-Marie-Tooth disease, type 1C 601098
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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