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Multiple congenital anomalies, hypotonia, seizures syndrome type 2
disorderSNOMED 773643006CUI C4751110
Overview
Multiple congenital anomalies, hypotonia, seizures syndrome type 2 is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
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Developmental hereditary disorder(parent)
X-linked recessive hereditary disease(parent)
Inherited metabolic disorder of nervous system(parent)
DEE - developmental and epileptic encephalopathy(parent)
Quick Facts
- SNOMED CT
- 773643006
- UMLS CUI
- C4751110
- Fully Specified Name
- Multiple congenital anomalies, hypotonia, seizures syndrome type 2 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.