OBO ID: DOID:0050541
Term Name: Charcot-Marie-Tooth disease type 4 Search Ontology:
Synonyms:
  • hereditary motor and sensory neuropathy
  • hereditary motor and sensory neuropathy Russe type
Definition: A Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance. http://www.ninds.nih.gov/disorders/charcot_marie_tooth/detail_charcot_marie_tooth.htm
References:
  • GARD:12440
  • ORDO:64749
Ontology: Human Disease   ( DOID:0050541 )
Relationships
is a type of:
has subtype:
OTHER Charcot-Marie-Tooth disease type 4 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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.