Decreased forced vital capacity
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:
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
Myosclerosis | (Orphanet:289380) |