Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Dec 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5159417014 | Genetic non-syndromic obesity (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 5159418016 | Genetic non-syndromic obesity | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Genetic non-syndromic obesity | Is a | Genetic disease | true | Inferred relationship | Existential restriction modifier | ||
| Genetic non-syndromic obesity | Interprets | Measured body weight | true | Inferred relationship | Existential restriction modifier | 1 | |
| Genetic non-syndromic obesity | Has interpretation | Above reference range | true | Inferred relationship | Existential restriction modifier | 1 | |
| Genetic non-syndromic obesity | Is a | Childhood obesity | true | Inferred relationship | Existential restriction modifier | ||
| Genetic non-syndromic obesity | Occurrence | Childhood | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital leptin deficiency | Is a | True | Genetic non-syndromic obesity | Inferred relationship | Existential restriction modifier | |
| Obesity due to centrosomal protein 19 deficiency | Is a | True | Genetic non-syndromic obesity | Inferred relationship | Existential restriction modifier | |
| Severe early-onset obesity insulin resistance syndrome due to SH2B adaptor protein 1 deficiency | Is a | True | Genetic non-syndromic obesity | Inferred relationship | Existential restriction modifier | |
| Obesity due to SIM bHLH transcription factor 1 deficiency | Is a | True | Genetic non-syndromic obesity | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR