OMOP Concept 37470524
Genetic childhood obesity disorder
StandardConditionSNOMED1359760004Disorder
Maps from
0
Descendants
17
Valid from
1 Apr 2025
Valid to
31 Dec 2099
OMOP concepts
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Synonyms
Alternative names recorded for Genetic childhood obesity disorder across source vocabularies.
- Genetic childhood obesity disorder (disorder)
- trastorno genético de obesidad en la infancia
- trastorno genético de obesidad en la infancia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(17)Included automatically when you query with descendants.
- 1Common polygenetic childhood obesity
- 1Genetic non-syndromic childhood obesity
- 1Genetic syndromic childhood obesity
- 2Acrocephalopolysyndactyly type II
- 2Alstrom syndrome
- 2Bardet-Biedl syndrome
- 2Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome
- 2Cohen syndrome
- 2Congenital leptin deficiency
- 2Intellectual disability, seizures, macrocephaly, obesity syndrome
- 2Obesity due to CEP19 deficiency
- 2Obesity due to SIM1 deficiency
- 2Prader-Willi syndrome
- 2Pseudohypoparathyroidism type I A
- 2Rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation syndrome
- 2Severe early-onset obesity insulin resistance syndrome due to SH2B1 deficiency
- 2SIM1-related Prader-Willi-like syndrome
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