Type 1 muscle fiber atrophy

Symptom Information:

Symptom ID: HPO:0011807
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Muscle fiber 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)
             Abnormality of muscle fibers(HPO:0004303)
                Muscle fiber atrophy(HPO:0100295)
                   Type 1 muscle fiber atrophy(HPO:0011807)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Combined oxidative phosphorylation defect type 8 (Orphanet:319504)
[DEL]EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED (OMIM:310300)