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 |
| 3642777016 | Hyperphalangy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3642781016 | Supernumerary phalanx (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3642782011 | Supernumerary phalanx | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5404101015 | Hyperphalangy is a congenital, non-syndromic limb malformation characterized by the presence of an accessory phalanx between metacarpal/metatarsal and proximal phalanx, or between any two other phalanges of a digit, excluding the thumb. Hyperphalangy is almost always bilateral, and patients present no more than five digits and no other skeletal anomalies. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5404102010 | Hyperphalangy is a congenital, non-syndromic limb malformation characterised by the presence of an accessory phalanx between metacarpal/metatarsal and proximal phalanx, or between any two other phalanges of a digit, excluding the thumb. Hyperphalangy is almost always bilateral, and patients present no more than five digits and no other skeletal anomalies. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hyperphalangy | Is a | Congenital anomaly of skeletal bone | true | Inferred relationship | Some | ||
| Hyperphalangy | Is a | Polydactyly (disorder) | true | Inferred relationship | Some | ||
| Hyperphalangy | Associated morphology | Supernumerary structure | true | Inferred relationship | Some | 1 | |
| Hyperphalangy | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Hyperphalangy | Finding site | Phalanx structure | true | Inferred relationship | Some | 1 | |
| Hyperphalangy | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Finger hyperphalangy, toe anomalies, severe pectus excavatum syndrome (disorder) | Is a | True | Hyperphalangy | Inferred relationship | Some | |
| Triphalangeal thumb | Is a | True | Hyperphalangy | Inferred relationship | Some | |
| Triphalangeal great toe | Is a | True | Hyperphalangy | Inferred relationship | Some |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR