Facial asymmetry, mild
Symptom Information:
Symptom ID: | OMIM : No Id available | |||
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Database Frequency: | 5 / 7739 | |||
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All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
OSTEOGENESIS IMPERFECTA, TYPE XII | (OMIM:613849) |
Trismus - pseudocamptodactyly | (Orphanet:3377) |