Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3655780019 | Inherited isolated adrenal insufficiency due to partial cytochrome P450 family 11 subfamily A member 1 deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3655781015 | Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3655782010 | Inherited isolated adrenal insufficiency due to partial cytochrome P450 family 11 subfamily A member 1 deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3655783017 | A rare genetic chronic primary adrenal insufficiency disorder due to partial loss-of-function CYP11A1 mutations. The disease has characteristics of early-onset adrenal insufficiency without associated abnormal external male genitalia. Patients present with signs of adrenal crisis, including electrolyte abnormalities, severe weakness, recurrent vomiting and seizures. Ultrasound reveals absent (or very small) adrenal glands. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | Is a | Congenital hypoplasia of adrenal gland | true | Inferred relationship | Some | ||
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Some | ||
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | Finding site | Adrenal cortex structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set