Developmental delay, mild to moderate
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 2 / 7739 | |
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All diseases associated with this symptom:
16p13.3 microduplication syndrome | (Orphanet:96078) |
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |