763715007: Familial hyperprolactinemia (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\Disorder of anterior pituitary\Hyperpituitarism\Hyperprolactinemia\Familial hyperprolactinemia
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\Disorder of anterior pituitary\Hyperpituitarism\Hyperprolactinemia\Familial hyperprolactinemia

\Finding of head and neck region\Head finding\...

\Finding of brain\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\Disorder of anterior pituitary\Hyperpituitarism\Hyperprolactinemia\Familial hyperprolactinemia

\Disorder of head\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\Disorder of anterior pituitary\Hyperpituitarism\Hyperprolactinemia\Familial hyperprolactinemia

\Functional finding\Increased hormone production\Hyperpituitarism\Hyperprolactinemia\Familial hyperprolactinemia

\Endocrine finding\Increased hormone production\Hyperpituitarism\Hyperprolactinemia\Familial hyperprolactinemia

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Familial hyperprolactinemia
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Familial hyperprolactinemia
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial hyperprolactinemia
\Disease\Disorder of embryonic structure\Disorder of hypothalamus\Disorder of pituitary gland\Disorder of anterior pituitary\Hyperpituitarism\Hyperprolactinemia\Familial hyperprolactinemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Familial hyperprolactinemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Familial hyperprolactinemia
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of pituitary gland\Disorder of anterior pituitary\Hyperpituitarism\Hyperprolactinemia\Familial hyperprolactinemia
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Familial hyperprolactinemia
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Familial hyperprolactinemia
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\Disorder of anterior pituitary\Hyperpituitarism\Hyperprolactinemia\Familial hyperprolactinemia
\Disease\Disorder of head\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\Disorder of anterior pituitary\Hyperpituitarism\Hyperprolactinemia\Familial hyperprolactinemia
\Disease\Familial disease\Familial hyperprolactinemia

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3643457015 Familial hyperprolactinemia en Synonym Active Entire term case insensitive SNOMED CT core module

3643458013 Familial hyperprolactinemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3643459017 Familial hyperprolactinaemia en Synonym Active Entire term case insensitive SNOMED CT core module

3643460010 Familial isolated prolactin receptor deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial hyperprolactinemia	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Familial hyperprolactinemia	Is a	Familial disease	true	Inferred relationship	Existential restriction modifier
Familial hyperprolactinemia	Is a	Hyperprolactinemia	true	Inferred relationship	Existential restriction modifier
Familial hyperprolactinemia	Is a	Hereditary disorder of endocrine system	true	Inferred relationship	Existential restriction modifier
Familial hyperprolactinemia	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
Familial hyperprolactinemia	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	1
Familial hyperprolactinemia	Finding site	Structure of pars distalis of pituitary	true	Inferred relationship	Existential restriction modifier	1
Familial hyperprolactinemia	Has interpretation	Increased	true	Inferred relationship	Existential restriction modifier	2
Familial hyperprolactinemia	Interprets	Hormone production, function	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3643457015	Familial hyperprolactinemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3643458013	Familial hyperprolactinemia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3643459017	Familial hyperprolactinaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3643460010	Familial isolated prolactin receptor deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module