Distal lower limb amyotrophy
Symptom Information:
Symptom ID: | HPO:0008944 | |||||||
Synonyms: |
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Cross references: |
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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) Lower limb amyotrophy(HPO:0007210) Distal lower limb amyotrophy(HPO:0008944) Distal amyotrophy(HPO:0003693) Distal lower limb amyotrophy(HPO:0008944) MedDRA: |
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Database Frequency: | 12 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Emery-Dreifuss muscular dystrophy | (Orphanet:98853) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | (Orphanet:93114) |
Autosomal dominant spastic paraplegia type 3 | (Orphanet:100984) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Behr syndrome | (Orphanet:1239) |
Cap myopathy | (Orphanet:171881) |
Charcot-Marie-Tooth disease type 4H | (Orphanet:99954) |
Distal myopathy with posterior leg and anterior hand involvement | (Orphanet:63273) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
NEMALINE MYOPATHY 1 | (OMIM:609284) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |