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Ontology Browser

Term:
autosomal dominant limb-girdle muscular dystrophy type 3 (DOID:0110306)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
autosomal dominant Emery-Dreifuss muscular dystrophy 2  
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  
An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the HNRNPDL gene on chromosome 4q21. (DO)
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 4  
myofibrillar myopathy 3  
rippling muscle disease 2  

Synonyms
Exact Synonyms: LGMD1G ;   autosomal dominant limb-girdle muscular dystrophy type 1G ;   muscular dystrophy limb-girdle type 1G
Primary IDs: MESH:C563794
Alternate IDs: OMIM:609115 ;   RDO:0012962
Xrefs: ORDO:55596
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/24647604

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.