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 |
| 3431473013 | Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3431474019 | Mesoaxial synostotic syndactyly with phalangeal reduction syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3431475018 | Syndactyly Malik Percin type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3431476017 | Syndactyly type 9 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5403255016 | A rare non-syndromic syndactyly characterized by mesoaxial reduction of fingers, complete syndactyly of the 3rd and 4th fingers with synostoses of the corresponding metacarpals and associated single phalanges, malformed thumbs, and hypoplasia and clinodactyly of the 5th finger. Preaxial webbing of toes with terminal phalangeal hypoplasia of all toes has been reported in association. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5403256015 | A rare non-syndromic syndactyly characterised by mesoaxial reduction of fingers, complete syndactyly of the 3rd and 4th fingers with synostoses of the corresponding metacarpals and associated single phalanges, malformed thumbs, and hypoplasia and clinodactyly of the 5th finger. Preaxial webbing of toes with terminal phalangeal hypoplasia of all toes has been reported in association. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder) | Is a | Syndactyly (disorder) | true | Inferred relationship | Some | ||
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder) | Associated morphology | Congenital abnormal fusion | false | Inferred relationship | Some | 1 | |
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder) | Finding site | Digit structure | true | Inferred relationship | Some | 1 | |
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder) | Associated morphology | Abnormally fused structure (morphologic abnormality) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR