Disease #01341

Official abbreviation NMAN
Name neuromyotonia and axonal neuropathy, autosomal recessive (NMAN, Gamstorp-Wohlfart syndrome)
OMIM ID 137200
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene HINT1
Associated tissues -
Disease features autosomal recessive
Remarks -