Search Ontology:
Human Disease

Charcot-Marie-Tooth disease type 1C

Term ID
DOID:0110151
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.