Overview
Genetic obesity disorder is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Prader-Willi-like syndrome(child)
Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome(child)
Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome(child)
Choroideremia with deafness and obesity syndrome(child)
Syndromic X-linked intellectual disability type 7(child)
Wilson Turner syndrome(child)
Sengers Hamel Otten syndrome(child)
Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome(child)
Obesity due to prohormone convertase I deficiency(child)
MOMO syndrome(child)
Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome(child)
Obesity due to melanocortin 4 receptor deficiency(child)
Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome(child)
Obesity due to leptin receptor gene deficiency(child)
PHIP-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome(child)
Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome(child)
X-linked intellectual disability, short stature, overweight syndrome(child)
Clark Baraitser syndrome(child)
MYT1L-related Prader-Willi-like syndrome(child)
Early-onset obesity, hyperphagia, severe developmental delay syndrome(child)
Quick Facts
- SNOMED CT
- 1359741006
- UMLS CUI
- C6008360
- Fully Specified Name
- Genetic obesity disorder (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.