Related Conditions
Congenital leptin deficiency(child)
Obesity due to centrosomal protein 19 deficiency(child)
Severe early-onset obesity insulin resistance syndrome due to SH2B1 deficiency(child)
Obesity due to SIM bHLH transcription factor 1 deficiency(child)
Genetic childhood obesity disorder(parent)
Disorder of hypothalamus(parent)
Quick Facts
- SNOMED CT
- 1260139006
- UMLS CUI
- C5680229
- Fully Specified Name
- Genetic non-syndromic childhood obesity (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.