60877009: Hormone secretion, function (observable entity)

SNOMED CT Concept\Observable entity (observable entity)\...

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

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

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

Descriptions:

Id Description Lang Type Status Case? Module

101151019 Hormone secretion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1203960014 Hormone secretion, function (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2671865011 Hormone secretion, function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

47891000077111 sécrétion hormonale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hormone secretion	Is a	Endocrine function	true	Inferred relationship	Some
Hormone secretion	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
Hypoparathyroidism due to Wilson disease	Interprets	True	Hormone secretion	Inferred relationship	Some	1
Sanjad-Sakati syndrome (SSS), also known as hypoparathyroidism - intellectual disability-dysmorphism, is a rare multiple congenital anomaly syndrome, mainly occurring in the Middle East and the Arabian Gulf countries, characterized by intrauterine growth restriction at birth, microcephaly, congenital hypoparathyroidism (that can cause hypocalcemic tetany or seizures in infancy), severe growth retardation, typical facial features (long narrow face, deep-set eyes, beaked nose, floppy and large ears, long philtrum, thin lips and micrognathia), and mild to moderate intellectual deficiency. Ocular findings (i.e. nanophthalmos, retinal vascular tortuosity and corneal opacification/clouding) and superior mesenteric artery syndrome have also been reported. Although SSS shares the same locus with the autosomal recessive form of Kenny-Caffey syndrome, the latter differs from SSS by its normal intelligence and skeletal features.	Interprets	True	Hormone secretion	Inferred relationship	Some	3
A rare bone disease characterized by secondary hyperparathyroidism in patients with chronic renal failure, caused by improper treatment in the early stages of the disease with retention of phosphorus, vitamin D deficiency, and disturbed calcium-phosphorus metabolism, which result in increased parathyroid hormone levels. Patients present with short stature, severe changes of the skull and jaws as well as other skeletal deformities, dental anomalies, brown tumors in the mouth, hearing loss, and neuropsychiatric disorders.	Interprets	True	Hormone secretion	Inferred relationship	Some	3
Autosomal dominant familial isolated hypoparathyroidism	Interprets	False	Hormone secretion	Inferred relationship	Some	1
Autosomal recessive familial isolated hypoparathyroidism	Interprets	False	Hormone secretion	Inferred relationship	Some	1
A rare genetic disorder with difference of sex development characterized by primary amenorrhea, short stature, delayed bone age, decreased levels of estradiol, elevated levels of follicle-stimulating hormone and luteinizing hormone, absent or underdeveloped uterus and ovaries, delayed development of pubic and axillary hair, and normal 46,XX karyotype.	Interprets	True	Hormone secretion	Inferred relationship	Some	2
Hyperparathyroidism due to lithium therapy	Interprets	True	Hormone secretion	Inferred relationship	Some	3
A rare, genetic premature ovarian failure characterised by decreased, abnormal or loss of ovarian function prior to age 40 in women bearing a premutation in FMR1 gene. This is defined as an expansion of 55-200 CGG repeats in the 5' untranslated region of the FMR1 gene. Clinical features include irregular or absent menstrual cycles (amenorrhoea), irregular ovulation and altered hormone profile (hypooestrogenism, and elevated serum gonadotropin levels) associated to fragile X premutation. Most of the patients have fertility problems (subfertility or infertility) and undergo early menopause.	Interprets	True	Hormone secretion	Inferred relationship	Some	1
Postprocedural ovarian failure	Interprets	True	Hormone secretion	Inferred relationship	Some	1
Autosomal dominant hypocalcemia (disorder)	Interprets	True	Hormone secretion	Inferred relationship	Some	1
Female infertility due to ovarian failure (disorder)	Interprets	True	Hormone secretion	Inferred relationship	Some	1

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