Delayed psychomotor development, profound
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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MedDRA: |
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| Database Frequency: | 3 / 7739 | |
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All diseases associated with this symptom:
| ASPARAGINE SYNTHETASE DEFICIENCY | (OMIM:615574) |
| Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
| Pontocerebellar hypoplasia type 4 | (Orphanet:166063) |