Rimmed vacuoles

Symptom Information:

Symptom ID: HPO:0003805
Synonyms:
'rimmed vacuoles' on biopsy [HPO:0003805]
'rimmed' vacuoles on biopsy [HPO:0003805]
'Rimmed vacuoles' on biopsy [OMIM:'Rimmed vacuoles' on biopsy]
'Rimmed' vacuoles on biopsy [OMIM:'Rimmed' vacuoles on biopsy]
Rimmed vacuoles [OMIM:Rimmed vacuoles]
Quality:
Cross references:
OMIM: "'Rimmed vacuoles' on biopsy" [OMIM:'Rimmed vacuoles' on biopsy]
OMIM: "'Rimmed' vacuoles on biopsy" [OMIM:'Rimmed' vacuoles on biopsy]
OMIM: "Rimmed vacuoles" [OMIM:Rimmed vacuoles]
Is a (Direct Parents):
HPO         Abnormality of muscle fibers
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)
                Rimmed vacuoles(HPO:0003805)
MedDRA:
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

AMYOTROPHIC LATERAL SCLEROSIS 20 (OMIM:615426)
Autosomal dominant limb-girdle muscular dystrophy type 1A (Orphanet:266)
Autosomal dominant limb-girdle muscular dystrophy type 1D (Orphanet:34516)
Autosomal dominant limb-girdle muscular dystrophy type 1F (Orphanet:55595)
Autosomal dominant limb-girdle muscular dystrophy type 1G (Orphanet:55596)
Autosomal recessive limb-girdle muscular dystrophy type 2G (Orphanet:34514)
DPM3-CDG (Orphanet:263494)
Distal myopathy with early respiratory muscle involvement (Orphanet:34521)
Distal myopathy with vocal cord weakness (Orphanet:600)
Distal myopathy, Nonaka type (Orphanet:602)
Distal myopathy, Welander type (Orphanet:603)
INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE (OMIM:600737)
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 1 (OMIM:167320)
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 3 (OMIM:615424)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia (Orphanet:52430)
Inclusion body myositis (Orphanet:611)
MYOPATHY, DISTAL, 3 (OMIM:610099)
NONAKA MYOPATHY (OMIM:605820)
Oculopharyngodistal myopathy (Orphanet:98897)
Tibial muscular dystrophy (Orphanet:609)
VACUOLAR NEUROMYOPATHY (OMIM:601846)
X-linked myopathy with postural muscle atrophy (Orphanet:178461)