OMOP Concept 37470526
Genetic syndromic childhood obesity
StandardConditionSNOMED1359763002Disorder
Maps from
0
Descendants
10
Valid from
1 Apr 2025
Valid to
31 Dec 2099
OMOP concepts
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Synonyms
Alternative names recorded for Genetic syndromic childhood obesity across source vocabularies.
- Genetic syndromic childhood obesity (disorder)
- obesidad infantil sindrómica de causa genética
- obesidad infantil sindrómica de causa genética (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(11)Roll up to these when you need a wider cohort.
Narrower concepts
(10)Included automatically when you query with descendants.
- 1Acrocephalopolysyndactyly type II
- 1Alstrom syndrome
- 1Bardet-Biedl syndrome
- 1Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome
- 1Cohen syndrome
- 1Intellectual disability, seizures, macrocephaly, obesity syndrome
- 1Prader-Willi syndrome
- 1Pseudohypoparathyroidism type I A
- 1Rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation syndrome
- 1SIM1-related Prader-Willi-like syndrome
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