Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3308873013 | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3308874019 | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Due to | 21-hydroxylase deficiency | false | Inferred relationship | Existential restriction modifier | ||
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Is a | Congenital adrenal hyperplasia | true | Inferred relationship | Existential restriction modifier | ||
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Associated morphology | Congenital hyperplasia | false | Inferred relationship | Existential restriction modifier | 2 | |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 2 | |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Finding site | Adrenal cortex structure | false | Inferred relationship | Existential restriction modifier | 2 | |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Due to | Deficiency of steroid 21-monooxygenase | true | Inferred relationship | Existential restriction modifier | 2 | |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Finding site | Adrenal cortex structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Associated morphology | Hyperplasia | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Steroid 21-monooxygenase deficiency, simple virilizing type | Is a | True | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Inferred relationship | Existential restriction modifier | |
Steroid 21-monooxygenase deficiency, salt wasting type | Is a | True | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets