Delayed motor development, severe
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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HPO:
MedDRA: |
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| Database Frequency: | 1 / 7739 | |
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All diseases associated with this symptom:
| MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 5 | (OMIM:613153) |