Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3643457015 | Familial hyperprolactinemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3643458013 | Familial hyperprolactinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3643459017 | Familial hyperprolactinaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3643460010 | Familial isolated prolactin receptor deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3643461014 | A rare genetic endocrine disorder characterized by persistently high prolactin serum levels (not associated with gestation, puerperium, drug intake or pituitary tumor) in multiple affected family members. Clinically it manifests with signs usually observed in hyperprolactinemia, which are: secondary medroxyprogesterone acetate (MPA)-negative amenorrhea and galactorrhea in female patients, and hypogonadism and decreased testosterone level-driven sexual disfunction in male patients. Oligomenorrhea and primary infertility have also been reported in some female patients. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3643462019 | A rare genetic endocrine disorder characterised by persistently high prolactin serum levels (not associated with gestation, puerperium, drug intake or pituitary tumour) in multiple affected family members. Clinically it manifests with signs usually observed in hyperprolactinaemia, which are: secondary medroxyprogesterone acetate (MPA)-negative amenorrhoea and galactorrhoea in female patients, and hypogonadism and decreased testosterone level-driven sexual disfunction in male patients. Oligomenorrhoea and primary infertility have also been reported in some female patients. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial hyperprolactinemia | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Familial hyperprolactinemia | Is a | Familial disease | true | Inferred relationship | Some | ||
| Familial hyperprolactinemia | Is a | Hyperprolactinemia | true | Inferred relationship | Some | ||
| Familial hyperprolactinemia | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Familial hyperprolactinemia | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Familial hyperprolactinemia | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Familial hyperprolactinemia | Finding site | Structure of pars distalis of pituitary (body structure) | true | Inferred relationship | Some | 1 | |
| Familial hyperprolactinemia | Has interpretation | Increased | true | Inferred relationship | Some | 2 | |
| Familial hyperprolactinemia | Interprets | Hormone production | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR