Brachydactyly, 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 microduplication syndrome | (Orphanet:261272) |
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
Goldblatt syndrome | (Orphanet:166272) |
Hall-Riggs syndrome | (Orphanet:2107) |
Spondyloepimetaphyseal dysplasia, Pakistani type | (Orphanet:93282) |