Peroneal muscle atrophy

Symptom Information:

Symptom ID: HPO:0009049
Synonyms:
Peroneal atrophy [HPO:0009049]
Peroneal atrophy [OMIM:Peroneal atrophy]
Peroneal muscle atrophy [OMIM:Peroneal muscle atrophy]
Quality:
Cross references:
OMIM: "Peroneal atrophy" [OMIM:Peroneal atrophy]
OMIM: "Peroneal muscle atrophy" [OMIM:Peroneal muscle atrophy]
Is a (Direct Parents):
HPO         Abnormality of the calf musculature
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 calf musculature(HPO:0001430)
                            Peroneal muscle atrophy(HPO:0009049)
       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 calf musculature(HPO:0001430)
                   Peroneal muscle atrophy(HPO:0009049)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM (OMIM:118301)
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE (OMIM:118230)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)
SCAPULOPERONEAL SYNDROME, NEUROGENIC, KAESER TYPE (OMIM:181400)
SPINAL MUSCULAR ATROPHY, SCAPULOPERONEAL (OMIM:271220)
Scapuloperoneal amyotrophy (Orphanet:85146)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)