Muscle biopsies show variation in fibrodiameter, internal nuclei, atrophy of type I fibers, focal loss of cross- striations, and cores of myofibrillar disruption with associated absence of mitochondria
Symptom Information:
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Symptom ID:
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OMIM : No Id available
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Synonyms:
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Quality:
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Cross references:
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| OMIM: "Muscle biopsies show variation in fibrodiameter, internal nuclei, atrophy of type I fibers, focal loss of cross- striations, and cores of myofibrillar disruption with associated absence of mitochondria" [OMIM:Muscle biopsies show variation in fibrodiameter, internal nuclei, atrophy of type I fibers, focal loss of cross- striations, and cores of myofibrillar disruption with associated absence of mitochondria] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
MedDRA:
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Database Frequency:
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1 / 7739
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Resource:
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All diseases associated with this symptom:
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Intellectual deficit - myopathy - short stature - endocrine defect
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(Orphanet:3068)
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