Profound global developmental delay
Symptom Information:
Symptom ID: | HPO:0012736 | |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 3 / 7739 | |
Resource: | HPO |
All diseases associated with this symptom:
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Pitt-Hopkins-like syndrome 2 | (OMIM:614325) |
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES | (OMIM:615789) |