Disease #00571 (CMS1B (myasthenic syndrome, congenital, type 1B, fast-channel (CMS-1B)), OMIM:608930)

Official abbreviation CMS1B
Name myasthenic syndrome, congenital, type 1B, fast-channel (CMS-1B)
OMIM ID 608930
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CHRNA1
Associated tissues -
Disease features -
Remarks -