Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
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 | SNOMED CT core module |
| 3431474019 | Mesoaxial synostotic syndactyly with phalangeal reduction syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3431475018 | Syndactyly Malik Percin type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3431476017 | Syndactyly type 9 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome | Is a | Syndactyly | true | Inferred relationship | Existential restriction modifier | ||
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome | Associated morphology | Congenital abnormal fusion | true | Inferred relationship | Existential restriction modifier | 1 | |
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome | Finding site | Digit structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Mesoaxial synostotic syndactyly with phalangeal reduction syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR