BabelNet

bn:05504712n

Noun Named Entity

No term available

Autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the gene encoding fukutin (FKTN) on chromosome 9q31 Wikidata

Relations

Sources

IS A

doença rara

GENETIC ASSOCIATION

FKTN

HEALTH SPECIALTY

neurologia