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Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome
disorderSNOMED 782825008CUI C5190632
Overview
Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Recessive hereditary disorder (autosomal)(parent)
Hereditary disorder of nervous system(parent)
Global developmental delay(parent)
Permanent diabetes mellitus of infancy(parent)
Hereditary disorder of endocrine system(parent)
Developmental hereditary disorder(parent)
Congenital microcephalus(parent)
DEE - developmental and epileptic encephalopathy(parent)
Quick Facts
- SNOMED CT
- 782825008
- UMLS CUI
- C5190632
- Fully Specified Name
- Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome (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.