Normal development
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Beta-ureidopropionase deficiency | (Orphanet:65287) |
Choanal atresia - deafness - cardiac defects - dysmorphism | (Orphanet:1200) |
Craniofacial dyssynostosis | (Orphanet:1516) |
Isolated congenital hypoglossia/aglossia | (Orphanet:141152) |