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113331007: Structure of endocrine system (body structure)

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
187172011 Endocrine system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
383266016 Endocrine structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
383267013 Endocrine system structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2638112015 Structure of endocrine system (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2642208013 Structure of endocrine system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
187172011 Endocrine system en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
187172011 Endocrine system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
383266016 Endocrine structure en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
383266016 Endocrine structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
383267013 Endocrine system structure en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
383267013 Endocrine system structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
648723016 Endocrine structure (body structure) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2638112015 Structure of endocrine system (body structure) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2638112015 Structure of endocrine system (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2642208013 Structure of endocrine system en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2642208013 Structure of endocrine system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
303291000077110 structure du système endocrinien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
303291000077110 structure du système endocrinien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

544 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure of endocrine system (body structure) Is a Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Structure of endocrine system (body structure) partie de Entire body as a whole (body structure) false Additional relationship (core metadata concept) Existential restriction modifier (core metadata concept)
Structure of endocrine system (body structure) Is a Structure of breast and/or endocrine system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Fetal virilism Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetal endocrine disorder Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Ketosis-prone diabetes mellitus Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Iatrogenic hypoglycaemia Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Pre-existing malnutrition-related diabetes mellitus in pregnancy (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Normal hormonal activity Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Normal hormone production (finding) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Deficiency of leukotriene C4 synthase Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Fetal virilism Finding site False Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Syndrome of infant of diabetic mother (disorder) Finding site False Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Transitory metabolic disturbance in infant of pre-diabetic mother (disorder) Finding site False Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Perinatal disorder of glucose regulation of fetus and/or neonate Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Perinatal thyroid disorder of fetus and/or neonate (disorder) Finding site False Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Transient hypothyroxinemia Finding site False Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Perinatal endocrine and metabolic disorders Finding site False Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Syndrome of infant of mother with gestational diabetes Finding site False Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypothyroxinaemia of prematurity Finding site False Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Transitory metabolic disturbance in infant of pre-diabetic mother (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Multiple paraganglioma associated with polycythemia Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare ophthalmic disorder characterized by clinical signs of Graves orbitopathy (unilateral or bilateral lid retraction, exophthalmos, soft tissue involvement, restrictive myopathy, and/or optic neuropathy) with normal thyroid function and without any signs of hyperthyroidism. Laboratory examination typically reveals low serum levels of thyroid-stimulating hormone receptor autoantibodies. Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal semi-dominant severe lipodystrophic laminopathy (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 4
A rare, genetic lipodystrophy characterised by abnormal subcutaneous fat distribution, resulting in preservation of visceral, neck and axillary fat and absence of lower limb and femoro gluteal subcutaneous fat. Additional clinical features are acanthosis nigricans, insulin-resistant type II diabetes mellitus, dyslipidemia, and hypertension, leading to pancreatitis, hepatomegaly and hepatic steatosis. Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
LIPE-related familial partial lipodystrophy Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Peroxisome proliferator activated receptor gamma-related familial partial lipodystrophy (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 4
A rare familial partial lipodystrophy characterized by adult onset of distal lipoatrophy and severe insulin resistance in the liver and peripheral tissues, hyperinsulinemia, and diabetes mellitus. Acanthosis nigricans and hypertension have been reported in association. Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 4
Fulminant type 1 diabetes mellitus (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Ketosis-resistant diabetes mellitus Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Psychogenic endocrine malfunction (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Alopecia due to thyroid disorder Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypothalamic adipsic hypernatremia syndrome (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 4
Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 4
Paracentesis of endocrine organ Procedure site - Direct (attribute) True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Paracentesis of endocrine organ Procedure site - Indirect (attribute) True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Carcinoid syndrome (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Wolfram syndrome (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare genetic endocrine disorder with characteristics of type 1 diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs. Type 1 has onset in the first decade with diabetes mellitus and optic atrophy manifestations. 50% of patients also develop diabetes insipidus. Additional features may include urinary tract abnormalities, neurological involvement and psychiatric manifestations. Caused by caused by homozygous or compound heterozygous mutation in the gene encoding wolframin (WFS1) on chromosome 4p16. Transmission is autosomal recessive. Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 4
Wolfram syndrome type 2 Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 4
Nuclear medicine diagnostic procedure on endocrine system Procedure site - Direct (attribute) False Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Presymptomatic diabetes mellitus type 1 (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Nocturnal hypoglycemia (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Unstable type I diabetes mellitus (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Brittle type 2 diabetes mellitus (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Frequent, clinically significant fluctuations in blood glucose levels both above and below levels expected to be achieved by available therapies. Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Type I diabetes mellitus in which the blood glucose levels over time exceed levels such that tests that reflect long-term variation of blood glucose, such as HbA1c, exceed limits that are expected to be achieved by available therapies. Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Uncontrolled gestational diabetes mellitus (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Uncontrolled type 2 diabetes mellitus (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Newly diagnosed type 1 diabetes mellitus Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Well controlled type 2 diabetes mellitus (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Well controlled type 1 diabetes mellitus Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Type 2 diabetes mellitus controlled by diet Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 2
Disorder due to well controlled type 2 diabetes mellitus (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 3
Newly diagnosed diabetes Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) Finding site True Structure of endocrine system (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1

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