Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3481746014 | Growth delay due to insulin-like growth factor type 1 deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3481747017 | Growth delay due to insulin-like growth factor type 1 deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3481748010 | Growth delay, deafness, intellectual disability syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3481749019 | IGF-1 (insulin-like growth factor 1) deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3481750019 | Primary insulin-like growth factor deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5403325014 | Growth delay due to insulin-like growth factor I deficiency is characterized by the association of intrauterine and postnatal growth retardation with sensorineural deafness and intellectual deficit. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5403326010 | Growth delay due to insulin-like growth factor I deficiency is characterised by the association of intrauterine and postnatal growth retardation with sensorineural deafness and intellectual deficit. | 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 type 1 deficiency (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Growth delay due to insulin-like growth factor type 1 deficiency (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | false | Inferred relationship | Some | ||
| Growth delay due to insulin-like growth factor type 1 deficiency (disorder) | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
| Growth delay due to insulin-like growth factor type 1 deficiency (disorder) | Is a | Growth hormone deficiency (disorder) | false | Inferred relationship | Some | ||
| Growth delay due to insulin-like growth factor type 1 deficiency (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Growth delay due to insulin-like growth factor type 1 deficiency (disorder) | Finding site | Structure of pars distalis of pituitary (body structure) | true | Inferred relationship | Some | 1 | |
| Growth delay due to insulin-like growth factor type 1 deficiency (disorder) | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
| Growth delay due to insulin-like growth factor type 1 deficiency (disorder) | Is a | Hereditary growth hormone deficiency (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR