Myopathy, nonprogressive
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Database Frequency: | 3 / 7739 | ||
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All diseases associated with this symptom:
Combined immunodeficiency due to ORAI1 deficiency | (Orphanet:317428) |
Combined immunodeficiency due to STIM1 deficiency | (Orphanet:317430) |
MYOPATHY, CONGENITAL | (OMIM:255300) |