Proximal upper limb amyotrophy

Symptom Information:

Symptom ID: HPO:0008948
Synonyms:
Proximal muscle atrophy in upper limbs [HPO:0008948]
Proximal upper limb muscle atrophy [HPO:0008948]
Proximal muscle atrophy in upper limbs [OMIM:Proximal muscle atrophy in upper limbs]
Proximal upper limb muscle atrophy [OMIM:Proximal upper limb muscle atrophy]
Quality:
Cross references:
OMIM: "Proximal muscle atrophy in upper limbs" [OMIM:Proximal muscle atrophy in upper limbs]
OMIM: "Proximal upper limb muscle atrophy" [OMIM:Proximal upper limb muscle atrophy]
Is a (Direct Parents):
HPO         Proximal amyotrophy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Skeletal muscle atrophy(HPO:0003202)
                Proximal amyotrophy(HPO:0007126)
                   Proximal upper limb amyotrophy(HPO:0008948)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant limb-girdle muscular dystrophy type 1G (Orphanet:55596)
Autosomal recessive limb-girdle muscular dystrophy type 2B (Orphanet:268)
Autosomal recessive limb-girdle muscular dystrophy type 2G (Orphanet:34514)