Nemaline bodies

Symptom Information:

Symptom ID: HPO:0003798
Synonyms:
Nemaline rods [HPO:0003798]
Nemaline rods [OMIM:Nemaline rods]
Nemaline rods (rare) [OMIM:Nemaline rods (rare)]
Quality:
Cross references:
OMIM: "Nemaline rods" [OMIM:Nemaline rods]
OMIM: "Nemaline rods (rare)" [OMIM:Nemaline rods (rare)]
Is a (Direct Parents):
HPO         Muscle fiber cytoplasmatic inclusion bodies
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 inclusion bodies(HPO:0100299)
                   Muscle fiber cytoplasmatic inclusion bodies(HPO:0100303)
                      Nemaline bodies(HPO:0003798)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2E (Orphanet:99939)
CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS (OMIM:606842)
Cap myopathy (Orphanet:171881)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Moderate multiminicore disease with hand involvement (Orphanet:178145)
NEMALINE MYOPATHY 2 (OMIM:256030)
NEMALINE MYOPATHY 4 (OMIM:609285)
NEMALINE MYOPATHY 5 (OMIM:605355)
NEMALINE MYOPATHY 6 (OMIM:609273)
NEMALINE MYOPATHY 7 (OMIM:610687)
NEMALINE MYOPATHY 8 (OMIM:615348)
Nemaline myopathy (Orphanet:607)