Proximal lower limb amyotrophy

Symptom Information:

Symptom ID: HPO:0008956
Synonyms:
Amyotrophy involving the thigh [HPO:0008956]
Amyotrophy of the thigh musculature [HPO:0008956]
Proximal lower limb muscle atrophy [HPO:0008956]
Thigh muscle atrophy [HPO:0008956]
Proximal lower limb muscle atrophy [OMIM:Proximal lower limb muscle atrophy]
Quality:
Cross references:
OMIM: "Proximal lower limb muscle atrophy" [OMIM:Proximal lower limb muscle atrophy]
Is a (Direct Parents):
HPO         Proximal amyotrophy
HPO         Abnormality of the musculature of the thigh
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the musculature of the limbs(HPO:0009127)
                      Abnormality of the musculature of the lower limbs(HPO:0001437)
                         Abnormality of the musculature of the thigh(HPO:0001441)
                            Proximal lower limb amyotrophy(HPO:0008956)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of the musculature of the limbs(HPO:0009127)
             Abnormality of the musculature of the lower limbs(HPO:0001437)
                Abnormality of the musculature of the thigh(HPO:0001441)
                   Proximal lower limb amyotrophy(HPO:0008956)
          Abnormality of muscle morphology(HPO:0011805)
             Skeletal muscle atrophy(HPO:0003202)
                Proximal amyotrophy(HPO:0007126)
                   Proximal lower limb amyotrophy(HPO:0008956)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures (Orphanet:209341)
Autosomal dominant congenital benign spinal muscular atrophy (Orphanet:1216)
Autosomal dominant limb-girdle muscular dystrophy type 1B (Orphanet:264)
Autosomal dominant limb-girdle muscular dystrophy type 1G (Orphanet:55596)
Duchenne muscular dystrophy (Orphanet:98896)