OBO ID: DOID:0080068
Term Name: Charcot-Marie-Tooth disease type 6 Search Ontology:
Synonyms:
  • hereditary motor and sensory neuropathy type 6
Definition: A Charcot-Marie-Tooth disease that is characterized by early-onset optic atrophy resulting in progressive visual loss and peripheral axonal sensorimotor neuropathy with highly variable age at onset and severity. (2)
References:
Ontology: Human Disease   ( DOID:0080068 )
OTHER Charcot-Marie-Tooth disease type 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MFN2 Hereditary motor and sensory neuropathy VIA 601152
SLC25A46 Neuropathy, hereditary motor and sensory, type VIB 616505
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None