Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3323395011 | Lymphedema hypoparathyroidism syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3323396012 | Lymphedema hypoparathyroidism syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3323397015 | Lymphoedema hypoparathyroidism syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3323398013 | Dahlberg Borer Newcomer syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3323399017 | Dahlberg syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3323400012 | A very rare ectodermal dysplasia syndrome, described in 2 adult brothers, characterized by the association of hypoparathyroidism, nephropathy, congenital lymphedema, mitral valve prolapse and brachytelephalangy. Additional features include mild facial dysmorphism, hypertrichosis and nail abnormalities. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3323401011 | A very rare ectodermal dysplasia syndrome, described in 2 adult brothers, characterised by the association of hypoparathyroidism, nephropathy, congenital lymphoedema, mitral valve prolapse and brachytelephalangy. Additional features include mild facial dysmorphism, hypertrichosis and nail abnormalities. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
13985751000172119 | syndrome de lymphœdème et hypoparathyroïdie | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
13985761000172117 | syndrome de Dahlberg-Borer-Newcomer | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4682381000172118 | syndroom van lymfoedeem en hypoparathyreoïdie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4682391000172115 | syndroom van lymfoedeem en hypoparathyroïdie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4682401000172118 | syndroom van Dahlberg | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4682411000172115 | syndroom van Dahlberg-Borer-Newcomer | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Lymphedema hypoparathyroidism syndrome (disorder) | Associated morphology | Lymphatic edema | false | Inferred relationship | Some | ||
Lymphedema hypoparathyroidism syndrome (disorder) | Is a | Ectodermal dysplasia | true | Inferred relationship | Some | ||
Lymphedema hypoparathyroidism syndrome (disorder) | Is a | Hypoparathyroidism | true | Inferred relationship | Some | ||
Lymphedema hypoparathyroidism syndrome (disorder) | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
Lymphedema hypoparathyroidism syndrome (disorder) | Is a | Hereditary lymphedema | true | Inferred relationship | Some | ||
Lymphedema hypoparathyroidism syndrome (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
Lymphedema hypoparathyroidism syndrome (disorder) | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
Lymphedema hypoparathyroidism syndrome (disorder) | Finding site | Parathyroid structure | false | Inferred relationship | Some | ||
Lymphedema hypoparathyroidism syndrome (disorder) | Has definitional manifestation | Decreased hormone secretion | false | Inferred relationship | Some | ||
Lymphedema hypoparathyroidism syndrome (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 5 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 5 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Finding site | Ectoderm structure | false | Inferred relationship | Some | 5 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 6 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 6 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 6 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Associated morphology | Lymphatic edema | true | Inferred relationship | Some | 1 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Finding site | Parathyroid structure | false | Inferred relationship | Some | 2 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Interprets | Hormone secretion | true | Inferred relationship | Some | 3 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 3 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 2 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 5 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Finding site | Parathyroid structure | true | Inferred relationship | Some | 5 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 4 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 4 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Finding site | Ectoderm structure | true | Inferred relationship | Some | 4 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 4 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Is a | Developmental hereditary disorder | false | Inferred relationship | Some | ||
Lymphedema hypoparathyroidism syndrome (disorder) | Is a | Congenital anomaly of limb | true | Inferred relationship | Some | ||
Lymphedema hypoparathyroidism syndrome (disorder) | Finding site | Limb structure | true | Inferred relationship | Some | 1 | |
Lymphedema hypoparathyroidism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets