Distal upper limb amyotrophy

Symptom Information:

Symptom ID: HPO:0007149
Synonyms:
Distal upper limb muscle atrophy [HPO:0007149]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Upper limb amyotrophy
HPO         Distal amyotrophy
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 upper limb(HPO:0002817)
                      Upper limb amyotrophy(HPO:0009129)
                         Distal upper limb amyotrophy(HPO:0007149)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Skeletal muscle atrophy(HPO:0003202)
                Distal amyotrophy(HPO:0003693)
                   Distal upper limb amyotrophy(HPO:0007149)
                Upper limb amyotrophy(HPO:0009129)
                   Distal upper limb amyotrophy(HPO:0007149)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (Orphanet:93114)
Autosomal recessive spastic paraplegia type 43 (Orphanet:320370)
Distal myopathy with posterior leg and anterior hand involvement (Orphanet:63273)
OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE (OMIM:258650)