OMOP Concept 40481140
Childhood obesity
StandardConditionSNOMED444862003Disorder
Maps from
6
Descendants
18
Valid from
31 Jul 2010
Valid to
31 Dec 2099
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Source codes that map to this concept
6 source codes normalize to Childhood obesity via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | Z68.54 | Body mass index [BMI] pediatric, 95th percentile for age to less than 120% of the 95th percentile for age | Non-standard |
| ICD10CM | Z68.55 | Body mass index [BMI] pediatric, 120% of the 95th percentile for age to less than 140% of the 95th percentile for age | Non-standard |
| ICD10CM | Z68.56 | Body mass index [BMI] pediatric, greater than or equal to 140% of the 95th percentile for age | Non-standard |
| ICD9CM | V85.54 | Body Mass Index, pediatric, greater than or equal to 95th percentile for age | Non-standard |
| MeSH | D063766 | Pediatric Obesity | Non-standard |
| Read | C380800 | Childhood obesity | Non-standard |
Synonyms
Alternative names recorded for Childhood obesity across source vocabularies.
- Childhood obesity BMI 95-100 percentile
- Childhood obesity (disorder)
- obesidad de la infancia
- obesidad de la infancia (trastorno)
- obesidad infantil
- obesidad infantil, índice de masa corporal en percentilos 95-100
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(18)Included automatically when you query with descendants.
- 1Genetic childhood obesity disorder
- 2Common polygenetic childhood obesity
- 2Genetic non-syndromic childhood obesity
- 2Genetic syndromic childhood obesity
- 3Acrocephalopolysyndactyly type II
- 3Alstrom syndrome
- 3Bardet-Biedl syndrome
- 3Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome
- 3Cohen syndrome
- 3Congenital leptin deficiency
- 3Intellectual disability, seizures, macrocephaly, obesity syndrome
- 3Obesity due to CEP19 deficiency
- 3Obesity due to SIM1 deficiency
- 3Prader-Willi syndrome
- 3Pseudohypoparathyroidism type I A
- 3Rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation syndrome
- 3Severe early-onset obesity insulin resistance syndrome due to SH2B1 deficiency
- 3SIM1-related Prader-Willi-like syndrome
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