BabelNet

bn:05495618n

Noun Named Entity

SYL

No term available

Autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the gene encoding protein O-mannosyltransferase (POMT1) Wikidata

Relations

Sources

IS A

rare disease

GENETIC ASSOCIATION

POMT1

HEALTH SPECIALTY

neurology