OBO ID: DOID:0110212
Term Name: Charcot-Marie-Tooth disease X-linked recessive 4 Search Ontology:
Synonyms:
  • axonal motor sensory neuropathy with deafness and mental retardation
  • Charcot-Marie-Tooth disease with deafness and mental retardation
  • CMT4X
  • CMTX4
  • NADMR
  • NAMSD
  • X-linked Charcot-Marie-Tooth disease type 4
Definition: A Charcot-Marie-Tooth disease X-linked that has_material_basis_in mutation in the AIFM1 gene on chromosome Xq26. https://www.ncbi.nlm.nih.gov/pubmed/23217327
References:
Ontology: Human Disease   ( DOID:0110212 )
Relationships
is a type of:
OTHER Charcot-Marie-Tooth disease X-linked recessive 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
AIFM1 Cowchock syndrome 310490
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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