OBO ID: DOID:0110196
Term Name: Charcot-Marie-Tooth disease type 4G Search Ontology:
Synonyms:
  • autosomal recessive Charcot-Marie-Tooth disease type 4G
  • Charcot-Marie-Tooth neuropathy type 4G
  • CMT4G
  • HMSNR
Definition: A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22. https://www.ncbi.nlm.nih.gov/pubmed/19536174
References:
Ontology: Human Disease   (DOID:0110196)
OTHER Charcot-Marie-Tooth disease type 4G PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
HK1 Neuropathy, hereditary motor and sensory, Russe type 605285
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None