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60877009: Hormone secretion, function (observable entity)

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
101151019 Hormone secretion en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
101151019 Hormone secretion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
799877016 Hormone secretion (function) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1203960014 Hormone secretion, function (observable entity) en Fully specified name Active Only initial character 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 Only initial character 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
47891000077111 sécrétion hormonale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hormone secretion Is a Endocrine function true Inferred relationship Existential restriction modifier (core metadata concept)
Hormone secretion Inheres in Structure of endocrine system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Normal hormone secretion Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Decreased hormone secretion Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Abnormal hormone secretion Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Increased hormone secretion Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Abnormal hormone secretion Interprets False Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Normal hormone secretion Interprets False Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Decreased hormone secretion Interprets False Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Increased hormone secretion Interprets False Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects. Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Iatrogenic ovarian failure Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Ovarian failure following radiotherapy Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 2
Primary ovarian failure Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Resistant ovary syndrome Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Pure gonadal dysgenesis 46,XX Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Ovarian failure Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Postablative ovarian failure Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Ovarian dysgenesis Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Menopause ovarian failure (disorder) Interprets False Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Post-chemotherapy ovarian failure Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Premature ovarian failure Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Autoimmune primary ovarian failure (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Secondary ovarian failure Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Iatrogenic premature ovarian failure Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired premature ovarian failure Interprets False Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic premature ovarian failure (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Premature ovarian failure due to autoimmune oophoritis (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare genetic disease characterized by sclerosing dysplasia affecting the diaphyseal and metaphyseal regions of the long bones, as well as the skull and metacarpals, in association with skin changes like those seen in ichthyosis vulgaris and premature ovarian failure with bilateral hypoplasia of the ovaries. Patients present in adulthood, primarily with swelling of the extremities and occasional mild pain in the legs. Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 2
Ovarian failure due to procedure (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Symptomatic postprocedural ovarian failure Interprets False Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Ectopic hyperparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperparathyroidism due to intestinal malabsorption Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperparathyroidism due to vitamin D deficiency (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypergonadism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary water-clear cell hyperplasia Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 2
hyperparathyroïdie causée par un traitement au lithium Interprets False Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Transient neonatal hyperparathyroidism (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Ovarian hyperfunction Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypersecretion of ovarian progesterone Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal severe primary hyperparathyroidism (NSHPT) is characterised by severe hypercalcaemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Secondary hyperparathyroidism of nonrenal origin (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial hyperparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperparathyroidism due to end stage renal disease on dialysis (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Ovarian hypersecretion Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Ovarian masculinisation syndrome Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Tertiary hyperparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Parathyromatosis Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Nephropathy, deafness, hyperparathyroidism syndrome Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal hyperparathyroidism (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperparathyroidism due to renal insufficiency Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypersecretion of ovarian androgens Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Ectopic parathyroid hormone-related protein secretion Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Secondary hyperparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Parathyroid hyperplasia Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 2
Primary hyperparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperparathyroidism-jaw tumor syndrome (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypoparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypomagnesemia with secondary hypocalcemia (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 3
Transitory neonatal hypoparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Secondary hypoparathyroidism (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism after external beam radiotherapy (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism due to hemochromatosis (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic parathyroidism Interprets False Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism, deafness, renal disease syndrome (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 5
Transient neonatal hypoparathyroidism due to maternal hyperparathyroidism (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Transient hypoparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal hypoparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic hypoparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism due to granulomatous disease (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism - X-linked Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism - autosomal dominant Interprets False Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Polyglandular autoimmune syndrome, type 1 Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Kenny syndrome Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypoparathyroidism after iodine thyroid ablation (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism due to impaired PTH secretion Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated late onset hypoparathyroidism (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated persistent neonatal hypoparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism following procedure (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Postablative hypoparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 2
Post-surgical hypoparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Autoimmune hypoparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Parathyroid hypocalcemic tetany Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare multiple congenital anomalies/dysmorphic syndrome characterized by the association of congenital hypoparathyroidism, nephropathy, congenital lymphedema, mitral valve prolapse and brachytelephalangy. Additional features include mild facial dysmorphism, hypertrichosis, and nail abnormalities. There have been no further descriptions in the literature since 1993. Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 3
Testicular hyperfunction Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 4
Gastrin secretion, function (observable entity) Is a True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept)
A rare hereditary familial primary hyperparathyroidism disease with characteristics of primary hyperparathyroidism due to single or multiple parathyroid tumours in at least two first-degree relatives in the absence of evidence of other endocrine disorders, tumours and/or systemic manifestations. Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudopseudohypoparathyroidism (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type II (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type I B Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type I A Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 2
Pseudohypoparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type 1C (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Normocalcemic primary hyperparathyroidism Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoparathyroidism following excision of thyroid gland (disorder) Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 2
Placental secretion of chorionic gonadotropin Is a True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept)
Ovarioleukodystrophy Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypoparathyroidism due to Wilson disease Interprets True Hormone secretion Inferred relationship Existential restriction modifier (core metadata concept) 1

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