Search Ontology:

Human Disease

autosomal dominant limb-girdle muscular dystrophy

Term ID

DOID:0110273

Synonyms

Definition

A limb-girdle muscular dystrophy that has_material_basis_in autosomal dominant inheritance. https://www.ncbi.nlm.nih.gov/pubmed/3275904

References

ICD10CM:G71.0
MIM:PS603511
ORDO:102014

Ontology

Human Disease ( DOID:0110273 )

Relationships

is a type of: autosomal dominant disease limb-girdle muscular dystrophy

autosomal dominant disease limb-girdle muscular dystrophy Show first 5 Terms
has subtype: autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3

autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models