Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1466162016 | Congenital pectus excavatum (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1485972017 | Congenital pectus excavatum | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1493805016 | Congenital funnel chest | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1440121000005115 | Kongenit pectus excavatum | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| objektivt: tragtbryst | Associated finding | False | Congenital pectus excavatum (disorder) | Inferred relationship | Some | 1 |
| objektivt: tragtbryst | Is a | False | Congenital pectus excavatum (disorder) | Inferred relationship | Some | |
| Pectus excavatum-macrocephaly-dysplastic nails syndrome is a rare multiple congenital anomalies syndrome characterized by relative macrocephaly, pectus excavatum, short stature, nail dysplasia, and motor developmental delay (that resolves during childhood). There have been no further descriptions in the literature since 1992. | Is a | True | Congenital pectus excavatum (disorder) | Inferred relationship | Some | |
| Finger hyperphalangy, toe anomalies, severe pectus excavatum syndrome (disorder) | Is a | True | Congenital pectus excavatum (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR