Aplasia of the musculature

Symptom Information:

Symptom ID: HPO:0100854
Synonyms:
Muscle agenesis [Orphanet:44250]
Muscle hypotrophy/atrophy/dystrophy/agenesis/amyotrophy [Orphanet:44250]
Quality:
Cross references:
Orphanet:44250 "Muscle hypotrophy/atrophy/dystrophy/agenesis/amyotrophy" [Orphanet:44250]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia involving the skeletal musculature
Orphanet Muscle anomalies
Orphanet 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)
             Aplasia/Hypoplasia involving the skeletal musculature(HPO:0001460)
                Aplasia of the musculature(HPO:0100854)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Carney complex (Orphanet:1359)
Kearns-Sayre syndrome (Orphanet:480)
Leprechaunism (Orphanet:508)
MELAS (Orphanet:550)
Mitochondrial myopathy and sideroblastic anemia (Orphanet:2598)
Steinert myotonic dystrophy (Orphanet:273)
Werner syndrome (Orphanet:902)