muscular dystrophy-dystroglycanopathy

Term ID

DOID:0112374

Synonyms

MDDG

Definition

A congenital muscular dystrophy characterized by muscular dystrophy resulting from defective glycosylation of dystroglycan. https://pubmed.ncbi.nlm.nih.gov/19299310/

References

ICD10CM:G71.2
ORDO:370953

Ontology

Human Disease ( DOID:0112374 )

Relationships

is a type of: congenital muscular dystrophy

congenital muscular dystrophy Show first 5 Terms
has subtype: congenital muscular dystrophy-dystroglycanopathy type A muscular dystrophy-dystroglycanopathy type B muscular dystrophy-dystroglycanopathy type C8 muscular dystrophy-dystroglycanopathy type C12

congenital muscular dystrophy-dystroglycanopathy type A muscular dystrophy-dystroglycanopathy type B muscular dystrophy-dystroglycanopathy type C8 muscular dystrophy-dystroglycanopathy type C12 Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models