Delayed development, severe
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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MedDRA: |
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| Database Frequency: | 2 / 7739 | |
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All diseases associated with this symptom:
| Congenital brain dysgenesis due to glutamine synthetase deficiency | (Orphanet:71278) |
| LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA | (OMIM:608809) |