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 |
3498437014 | Symphalangism with multiple anomalies of hands and feet | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3498438016 | Symphalangism with multiple anomalies of hands and feet syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3498439012 | Learman syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3498440014 | Symphalangism with multiple anomalies of hands and feet syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
6111081000146111 | syndroom van Learman | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6731131000146114 | syndroom van symfalangisme met meervoudige anomalieën van handen en voeten (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6731141000146118 | syndroom van symfalangisme met meervoudige anomalieën van handen en voeten | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
3499923019 | An exceedingly rare syndrome described in one family and with characteristics of proximal symphalangism and multiple hand and feet disorders (syndactyly, clinodactyly, hypoplasia of the thenar and hypothenar eminences and a distinctive dermatoglyphic pattern). There have been no further descriptions in the literature since 1981. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Symphalangism with multiple anomalies of hands and feet syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Symphalangism with multiple anomalies of hands and feet syndrome | Is a | Multiple malformation syndrome with limb defect as major feature | true | Inferred relationship | Some | ||
Symphalangism with multiple anomalies of hands and feet syndrome | Is a | Symphalangism | true | Inferred relationship | Some | ||
Symphalangism with multiple anomalies of hands and feet syndrome | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Symphalangism with multiple anomalies of hands and feet syndrome | Associated morphology | congenitale ankylose | false | Inferred relationship | Some | 1 | |
Symphalangism with multiple anomalies of hands and feet syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Symphalangism with multiple anomalies of hands and feet syndrome | Finding site | Interphalangeal joint structure (body structure) | true | Inferred relationship | Some | 1 | |
Symphalangism with multiple anomalies of hands and feet syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Symphalangism with multiple anomalies of hands and feet syndrome | Associated morphology | Ankylosis | true | Inferred relationship | Some | 1 | |
Symphalangism with multiple anomalies of hands and feet syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets