Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3303207018 | Growth delay due to insulin-like growth factor I resistance (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3303208011 | Growth delay due to insulin-like growth factor I resistance | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3303209015 | Growth delay due to insulin-like growth factor 1 resistance | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303210013 | IGF-1 (insulin-like growth factor 1) resistance | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3303211012 | Somatomedin C resistance | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 748041000241114 | retard de croissance par résistance au facteur de croissance analogue à l'insuline type 1 (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 915421000172114 | retard de croissance par résistance au facteur de croissance analogue à l'insuline type 1 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 964701000172114 | résistance à l'IGF-1 (insulin-like growth factor I) | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3302601019 | Variable intrauterine and postnatal growth retardation and elevated serum IGF-I levels. Additional features include variable degrees of intellectual deficit, microcephaly and dysmorphism (broad nasal bridge and tip, smooth philtrum, thin upper and everted lower lips, short fingers, clinodactyly, wide-set nipples and pectus excavatum). Prevalence is unknown, may be caused by a variety of genetic defects. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Growth delay due to insulin-like growth factor I resistance (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Growth delay due to insulin-like growth factor I resistance (disorder) | est un(e) (attribut) | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Growth delay due to insulin-like growth factor I resistance (disorder) | interprète (attribut) | Height / growth measure | true | Inferred relationship | Some | 2 | |
| Growth delay due to insulin-like growth factor I resistance (disorder) | est un(e) (attribut) | maladie héréditaire | false | Inferred relationship | Some | ||
| Growth delay due to insulin-like growth factor I resistance (disorder) | est un(e) (attribut) | insuffisance staturale | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR