Upper limb amyotrophy

Symptom Information:

Symptom ID: HPO:0009129
Synonyms:
Amyotrophy involving the upper limbs [HPO:0009129]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the upper limb
HPO         Skeletal muscle atrophy
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)
                Upper limb amyotrophy(HPO:0009129)
       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 upper limb(HPO:0002817)
                      Upper limb amyotrophy(HPO:0009129)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2D (Orphanet:99938)
Autosomal dominant spastic paraplegia type 10 (Orphanet:100991)
Friedreich ataxia 1 (OMIM:229300)