Mild prognathism
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:
AXENFELD-RIEGER SYNDROME, TYPE 2 | (OMIM:601499) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Craniometadiaphyseal dysplasia, wormian bone type | (Orphanet:85184) |