Distal upper limb amyotrophy
Symptom Information:
Symptom ID: | HPO:0007149 | ||||
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Is a (Direct Parents): |
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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) Distal amyotrophy(HPO:0003693) Distal upper limb amyotrophy(HPO:0007149) Upper limb amyotrophy(HPO:0009129) Distal upper limb amyotrophy(HPO:0007149) 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) MedDRA: |
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Database Frequency: | 4 / 7739 | ||||
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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) |