Showing entry for CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C



                               
General Disease Information
BXGD IdBXGD016411
Disease NameCHARCOT-MARIE-TOOTH DISEASE, TYPE 4C
Disease CUI IdC1866636
MeSH Codes C16   C10  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic disease; disease of anatomical entity
Disorder Network disorder-protein-compound-food associations