Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3308868019 | Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308869010 | Congenital lipoid adrenal hyperplasia due to STAR deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3308870011 | Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308871010 | One of the most severe forms of congenital adrenal hyperplasia, it is extremely rare. Congenital anomalies are typically seen in the perinatal period. Boys are not virilized and demonstrate a complete girl phenotype. The external genitalia of girls are normal. Hypoglycemic seizures, vomiting or symptoms of dehydration are common manifestations. This disease is due to a mutation in the STAR gene, which encodes for a protein that regulates steroid hormone synthesis. The disease follows an autosomal recessive pattern of inheritance. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308872015 | One of the most severe forms of congenital adrenal hyperplasia, it is extremely rare. Congenital anomalies are typically seen in the perinatal period. Boys are not virilised and demonstrate a complete girl phenotype. The external genitalia of girls are normal. Hypoglycaemic seizures, vomiting or symptoms of dehydration are common manifestations. This disease is due to a mutation in the STAR gene, which encodes for a protein that regulates steroid hormone synthesis. The disease follows an autosomal recessive pattern of inheritance. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3875581000052110 | medfödd lipoid binjurehyperplasi orsakad av brist på steroidogent akut regulatoriskt protein | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency (disorder) | Is a | Congenital adrenal hyperplasia | true | Inferred relationship | Some | ||
Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency (disorder) | Associated morphology | kongenital hyperplasi | false | Inferred relationship | Some | 1 | |
Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency (disorder) | Finding site | Adrenal cortex structure | true | Inferred relationship | Some | 1 | |
Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency (disorder) | Associated morphology | Hyperplasia | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency classic form (disorder) | Is a | True | Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency (disorder) | Inferred relationship | Some | |
Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency non classic form | Is a | True | Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency (disorder) | Inferred relationship | Some |
This concept is not in any reference sets