415691001: Sweating, function (observable entity)

SNOMED CT Concept\Observable entity (observable entity)\Any function or property that is not mainly morphologic or structural, including both measurable and observable features and physiologic actions\Function of the integumentary system\Skin function\Sweating, function (observable entity)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2531517012 Sweating, function (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2535048015 Sweating en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2537802012 Diaphoresis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2537803019 Hidropoiesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2537804013 Hidrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2537805014 Perspiration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2537806010 Sweating, function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

274661000077119 sudation 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
Sweating, function (observable entity)	Is a	Skin function	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Acquired anhidrosis co-occurrent and due to primary autonomic disorder (disorder)	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	4
Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome is a rare, genetic, syndromic intellectual disability disorder characterised by severe intellectual disability with significant speech and language impairment, hypohidrosis (often resulting in hyperthermia) with normal sweat gland appearance, tooth enamel hypoplasia, palmoplantar hyperkeratosis and a high frequency of acquired microcephaly. Mild facial dysmorphism, including lateral flaring of the eyebrows, broad nasal tip, and thick vermilion border, may also be observed.	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	6
Hypohidrosis due to genetic abnormality of eccrine gland structure and function (disorder)	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	2
Idiopathic pure sudomotor failure (disorder)	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	2
Hypohidrosis of unknown etiology (disorder)	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	2
Hypohidrosis co-occurrent and due to disorder of sympathetic nervous system (disorder)	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	1
A rare genetic skin disease characterized by congenital generalized anhidrosis resulting in severe heat intolerance, due to functionally impaired eccrine sweat production. Skin biopsy reveals normal morphology and number of sweat glands. Dental, hair, nail, or other skin or extracutaneous anomalies are absent.	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	2
A rare genetic disease characterised by abnormalities in renal ion transport, ectodermal gland homeostasis, and epidermal integrity, resulting in generalised hypohidrosis, heat intolerance, salt-losing nephropathy, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, and xerostomia. Development of nephrolithiasis and severe enamel wear have also been described. Laboratory findings include hypermagnesaemia, hypokalaemia, hypercalcaemia, and hypocalciuria.	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	3
Drug-induced hyperhidrosis	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	2
Hypohidrosis due to neurological disorder (disorder)	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	1
Localized hyperhidrosis due to focal neurological disorder (disorder)	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	1
Menopausal hyperhidrosis (disorder)	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	1
A rare hereditary sensory and autonomic neuropathy characterized by congenital insensitivity to pain, general hypesthesia, diminished temperature sensitivity, and hyperhidrosis. Motor function is preserved. Skin biopsy reveals lack of cutaneous innervation except for sensory and autonomic innervation of blood vessels and sweat glands.	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	1
A rare ectodermal dysplasia syndrome characterized by hypotrichosis, tooth enamel hypoplasia, hypoplastic nails, palmoplantar keratoderma, hyperhidrosis on hands, face, and scalp, bilateral partial cutaneous syndactyly, and dysmorphic facial features with large prominent ear pinnae, pointed nose, and thin upper lips. Association of cardiomegaly has also been reported.	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	9
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	5
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB gain of function mutation (disorder)	Interprets	True	Sweating, function (observable entity)	Inferred relationship	Some	4

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This concept is not in any reference sets