Showing entry for MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL

General Disease Information
BXGD Id	BXGD022108
Disease Name	MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL
Disease CUI Id	C4084823
MeSH Codes
Disease Class Name
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations