Flat facial profile
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 6 / 7739 | |
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All diseases associated with this symptom:
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Cleft lip/palate - intestinal malrotation - cardiopathy | (Orphanet:2001) |
Connective tissue disorder due to lysyl hydroxylase-3 deficiency | (Orphanet:300284) |
Craniofacial-deafness-hand syndrome | (Orphanet:1529) |
Down syndrome | (Orphanet:870) |