35188005: Hormone production, function (observable entity)

SNOMED CT Concept\Observable entity\...

\Clinical history/examination observable (observable entity)\Endocrine observable\Endocrine function\Hormone production

\Any function or property that is not mainly morphologic or structural, including both measurable and observable features and physiologic actions\Endocrine function\Hormone production

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hormone production	Is a	Endocrine function	true	Inferred relationship	Some
Hormone production	This attribute specifies the independent continuant which bears the quality, and on which the dependent quality (of this observable) depends.	Structure of endocrine system (body structure)	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Decreased hormone production	Interprets	True	Hormone production	Inferred relationship	Some	1
Normal hormone production	Interprets	True	Hormone production	Inferred relationship	Some	1
Abnormal hormone production	Interprets	True	Hormone production	Inferred relationship	Some	1
Increased hormone production	Interprets	True	Hormone production	Inferred relationship	Some	1
Increased hormone production	Interprets	False	Hormone production	Inferred relationship	Some	1
Abnormal hormone production	Interprets	False	Hormone production	Inferred relationship	Some	1
Decreased hormone production	Interprets	False	Hormone production	Inferred relationship	Some	1
Normal hormone production	Interprets	False	Hormone production	Inferred relationship	Some	1
Familial male limited precocious puberty (FMPP) is a gonadotropin-independent familial form of male-limited precocious puberty, generally presenting between 2-5 years of age as accelerated growth, early development of secondary sexual characteristics and reduced adult height.	Interprets	True	Hormone production	Inferred relationship	Some	3
Deficiency of testosterone biosynthesis	Interprets	True	Hormone production	Inferred relationship	Some	1
Hypothyroidism following radioiodine therapy	Interprets	True	Hormone production	Inferred relationship	Some	1
Iatrogenic testicular hypofunction	Interprets	True	Hormone production	Inferred relationship	Some	1
Leydig cell failure in adult	Interprets	True	Hormone production	Inferred relationship	Some	1
Testicular hypofunction (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	1
Hypothyroidism caused by radiation	Interprets	True	Hormone production	Inferred relationship	Some	1
Postablative testicular hypofunction	Interprets	True	Hormone production	Inferred relationship	Some	1
Post-chemotherapy testicular hypofunction	Interprets	True	Hormone production	Inferred relationship	Some	1
Postablative hypothyroidism	Interprets	True	Hormone production	Inferred relationship	Some	1
Testicular hypofunction due to defect in adrenocortical hormone synthesis	Interprets	True	Hormone production	Inferred relationship	Some	1
Primary testicular failure (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	1
Testicular hypofunction following procedure (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	1
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus.	Interprets	True	Hormone production	Inferred relationship	Some	2
testikulær hypofunktion efter strålebehandling	Interprets	False	Hormone production	Inferred relationship	Some	2
Hypothyroidism following external radiotherapy (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	2
Postablative hypoparathyroidism (disorder)	Interprets	False	Hormone production	Inferred relationship	Some	1
Adrenal hyperfunction	Interprets	True	Hormone production	Inferred relationship	Some	1
Catecholamine hypersecretion	Interprets	True	Hormone production	Inferred relationship	Some	1
Medulloadrenal hyperfunction	Interprets	True	Hormone production	Inferred relationship	Some	1
Adrenocortical hyperfunction	Interprets	True	Hormone production	Inferred relationship	Some	1
Familial hyperprolactinemia is a rare, genetic endocrine disorder characterized by persistently high prolactin serum levels (not associated with gestation, puerperium, drug intake or pituitary tumor) in multiple members of a family. 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 dysfunction in male patients. Oligomenorrhea and primary infertility have also been reported in some female patients.	Interprets	True	Hormone production	Inferred relationship	Some	2
Hyperpituitarism	Interprets	True	Hormone production	Inferred relationship	Some	1
Pituitary stalk compression hyperprolactinemia	Interprets	True	Hormone production	Inferred relationship	Some	1
Thyrotropin overproduction	Interprets	True	Hormone production	Inferred relationship	Some	1
Thyrotoxicosis due to inappropriate TSH secretion	Interprets	True	Hormone production	Inferred relationship	Some	1
Non-pregnancy related A-G syndrome	Interprets	True	Hormone production	Inferred relationship	Some	2
Gigantism due to somatostatin deficiency	Interprets	True	Hormone production	Inferred relationship	Some	1
Overproduction of growth hormone (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	1
X-linked intellectual disability-acromegaly-hyperactivity syndrome is characterized by severe intellectual deficit, acromegaly and hyperactivity. The syndrome has been described in two half-brothers. Dysarthria, aggressive behavior, a characteristic facies (an acromegalic and triangular face with a long nose) and macroorchidism were also present. The mother displayed moderate intellectual deficit and milder facial anomalies. Central nervous system anomalies were identified in the two boys: subarachnoid cysts and hyperdensity in the pontine region.	Interprets	True	Hormone production	Inferred relationship	Some	2
Hyperprolactinaemia	Interprets	True	Hormone production	Inferred relationship	Some	1
Idiopathic hyperprolactinaemia	Interprets	True	Hormone production	Inferred relationship	Some	1
Transient hyperprolactinemia	Interprets	True	Hormone production	Inferred relationship	Some	1
Drug-induced hyperprolactinaemia	Interprets	True	Hormone production	Inferred relationship	Some	1
Physiological hyperprolactinemia	Interprets	True	Hormone production	Inferred relationship	Some	1
Beckwith-Wiedemann syndrome	Interprets	True	Hormone production	Inferred relationship	Some	3
Transient infantile hyperthyrotropinemia (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	2
Acromegaly	Interprets	True	Hormone production	Inferred relationship	Some	1
Pregnancy hyperprolactinemia	Interprets	True	Hormone production	Inferred relationship	Some	1
ACTH hypersecretion not causing Cushing's syndrome	Interprets	True	Hormone production	Inferred relationship	Some	1
LH hypersecretion	Interprets	True	Hormone production	Inferred relationship	Some	1
Gonadotrophin hypersecretion	Interprets	True	Hormone production	Inferred relationship	Some	1
Hyperestrogenism	Interprets	True	Hormone production	Inferred relationship	Some	1
Sotos' syndrome	Interprets	True	Hormone production	Inferred relationship	Some	3
Pituitary dependent hypercortisolism	Interprets	True	Hormone production	Inferred relationship	Some	1
Hypersomatotropic gigantism	Interprets	True	Hormone production	Inferred relationship	Some	2
FSH hypersecretion	Interprets	True	Hormone production	Inferred relationship	Some	1
Eunuchoid gigantism	Interprets	True	Hormone production	Inferred relationship	Some	1
X-linked acrogigantism	Interprets	False	Hormone production	Inferred relationship	Some	3
Lactation hyperprolactinaemia	Interprets	True	Hormone production	Inferred relationship	Some	1
Thyrotoxicosis due to pituitary thyroid hormone resistance	Interprets	True	Hormone production	Inferred relationship	Some	2
Prepuberal hyperpituitarism	Interprets	True	Hormone production	Inferred relationship	Some	1
Adrenocorticotropic hormone hypersecretion (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	1
Macroprolactinemia (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	1
Thyrotoxicosis due to overproduction of thyroid stimulating hormone	Interprets	True	Hormone production	Inferred relationship	Some	1
Postpartum amenorrhoea-galactorrhea syndrome	Interprets	True	Hormone production	Inferred relationship	Some	2
Gigantism and acromegaly	Interprets	True	Hormone production	Inferred relationship	Some	1
Secondary hyperprolactinemia	Interprets	True	Hormone production	Inferred relationship	Some	1
Gigantism	Interprets	True	Hormone production	Inferred relationship	Some	1
Thyrotoxicosis due to TSHoma	Interprets	True	Hormone production	Inferred relationship	Some	1
Secondary hyperprolactinemia due to prolactin-secreting tumor (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	1
A rare genetic adrenal disorder with characteristics of congenital bronzed hyperpigmentation, cutis laxa of the hands and feet, body disproportion (comprising large hands, feet, nose and ears), hirsutism and severe intellectual disability. Patients additionally present hyperadrenocorticism, cushingoid features, premature adrenarche and diabetes mellitus, as well as skeletal deformities (not present at birth and which progress with age). There have been no further descriptions in the literature since 1981.	Interprets	True	Hormone production	Inferred relationship	Some	2
A rare genetic endocrine disease with characteristics of early-onset (before the age of five years old) excessive acceleration of linear growth and body size due to pituitary mixed growth hormone and prolactin secreting adenomas and/or mixed-cell pituitary hyperplasia. Patients present gigantism and may associate acromegalic features (for example coarse facial features, frontal bossing, prognathism, increased interdental space) as well as marked enlargement of hands and feet, soft tissue swelling, appetite increase and acanthosis nigricans.	Interprets	True	Hormone production	Inferred relationship	Some	2
A type of familial infantile gigantism caused by microduplication of Xq26.3. Onset usually occurs in the first year of life in previously normal infants. Patients present with gigantism and may associate acromegalic features (e.g. coarse facial features, frontal bossing, prognathism, increased interdental space) as well as marked enlargement of hands and feet, soft tissue swelling, appetite increase and acanthosis nigricans. May present as a sporadic condition or as familial isolated pituitary adenomas.	Interprets	True	Hormone production	Inferred relationship	Some	2
Precocious puberty with adrenocortical hyperfunction (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	2
Postsurgical testicular hypofunction	Interprets	True	Hormone production	Inferred relationship	Some	2
Hyperprolactinemia due to hypothyroidism	Interprets	True	Hormone production	Inferred relationship	Some	4
Male sexual precocity with adrenal hyperplasia (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	2
Testicular hypofunction due to and following radiotherapy (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	2
Hypothyroidism due to and following radiotherapy (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	4
Testicular hypofunction caused by ionizing radiation (disorder)	Interprets	True	Hormone production	Inferred relationship	Some	2

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
58718018	Hormone production	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1194553018	Hormone production, function (observable entity)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2670807011	Hormone production, function	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1994221000005111	Hormonproduktion	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)