Moderate global developmental delay
Symptom Information:
Symptom ID: | HPO:0011343 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of higher mental function(HPO:0011446) Cognitive impairment(HPO:0100543) Global developmental delay(HPO:0001263) Moderate global developmental delay(HPO:0011343) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Beckwith-Wiedemann syndrome due to NSD1 mutation | (Orphanet:238613) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Gordon syndrome | (Orphanet:376) |
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome | (Orphanet:457185) |