Search Ontology:
Human Disease

autosomal dominant limb-girdle muscular dystrophy type 1H

Term ID
DOID:0110303
Synonyms
  • LGMD1H
  • muscular dystrophy limb-girdle type 1H
Definition
An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in with variation in the region 3p25.1-p23. https://www.ncbi.nlm.nih.gov/pubmed/20068593
References
Ontology
Human Disease   ( DOID:0110303 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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