Internal nuclei
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 9 / 7739 | |
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All diseases associated with this symptom:
Autosomal dominant limb-girdle muscular dystrophy type 1D | (Orphanet:34516) |
Congenital myopathy with internal nuclei and atypical cores | (Orphanet:319160) |
MYOPATHY, DISTAL, TATEYAMA TYPE | (OMIM:614321) |
MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET | (OMIM:300718) |
MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE | (OMIM:300717) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
Myosclerosis | (Orphanet:289380) |
Vici syndrome | (Orphanet:1493) |
ZASP-related myofibrillar myopathy | (Orphanet:98912) |