Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3705326018 | Digital extensor muscle aplasia with polyneuropathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3705327010 | Digital extensor muscle aplasia with polyneuropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3705328017 | Polyneuropathy, hand defect syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3705329013 | Hamanishi Ueba Tsuji syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3705330015 | Congenital aplasia of extensor muscle of finger and thumb associated with generalized polyneuropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3705331016 | Congenital aplasia of extensor muscle of finger and thumb associated with generalised polyneuropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3705332011 | A rare hereditary motor and sensory neuropathy with characteristics of flexion deformities of the thumb and fingers, sensory deficit in the hand and polyneuropathic electrophysiologic findings in the limbs. Operation on the hands reveals extensor muscles and their tendons to be absent or hypoplastic. There have been no further descriptions in the literature since 1986. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
930711000172111 | aplasie des muscles extenseurs des doigts et pouce-polyneuropathie | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
968211000172113 | syndrome de Hamanishi-Ueba-Tsuji | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
990651000172113 | aplasie van vingerextensoren, polyneuropathie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
1008661000172118 | congenitale aplasie van strekspieren van vingers en duim geassocieerd met gegeneraliseerde polyneuropathie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Hereditary motor and sensory neuropathy (disorder) | true | Inferred relationship | Some | ||
Digital extensor muscle aplasia with polyneuropathy (disorder) | Finding site | Structure of extensor muscle of hand (body structure) | true | Inferred relationship | Some | 1 | |
Digital extensor muscle aplasia with polyneuropathy (disorder) | Associated morphology | Aplasia | true | Inferred relationship | Some | 1 | |
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Digital extensor muscle aplasia with polyneuropathy (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Combined disorder of muscle AND peripheral nerve (disorder) | true | Inferred relationship | Some | ||
Digital extensor muscle aplasia with polyneuropathy (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Digital extensor muscle aplasia with polyneuropathy (disorder) | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 2 | |
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Aplasia of muscle | true | Inferred relationship | Some | ||
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Congenital anomaly of skeletal muscle | false | Inferred relationship | Some | ||
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Polyneuropathy | true | Inferred relationship | Some | ||
Digital extensor muscle aplasia with polyneuropathy (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Digital extensor muscle aplasia with polyneuropathy (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Congenital anomaly of upper limb | false | Inferred relationship | Some | ||
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Absence of upper limb (finding) | false | Inferred relationship | Some | ||
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Congenital absence of part of upper limb | true | Inferred relationship | Some | ||
Digital extensor muscle aplasia with polyneuropathy (disorder) | Is a | Congenital absence of skeletal muscle | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets