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277879009: Autonomic neuropathy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2013. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
414606010 Autonomic neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
670968013 Autonomic neuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
937211000195113 neuropatia autonoma it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
352311000077110 neuropathie autonome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

96 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autonomic neuropathy Is a Neuropathy false Inferred relationship Some
Autonomic neuropathy Finding site Autonomic nerve structure true Inferred relationship Some 1
Autonomic neuropathy Is a Neuropathy (disorder) true Inferred relationship Some
Autonomic neuropathy Is a Disorder of the peripheral nervous system false Inferred relationship Some
Autonomic neuropathy Is a Disorder of autonomic nervous system true Inferred relationship Some
Autonomic neuropathy Is a Peripheral nerve finding false Inferred relationship Some
Autonomic neuropathy Is a Disorder of soft tissue false Inferred relationship Some
Autonomic neuropathy Is a Peripheral nerve disease false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
neuropathie autonome diabétique liée au diabète sucré de type 2 Is a False Autonomic neuropathy Inferred relationship Some
Diabetic autonomic neuropathy associated with type 1 diabetes mellitus Is a False Autonomic neuropathy Inferred relationship Some
Autonomic nerve injury Is a True Autonomic neuropathy Inferred relationship Some
Disorder of peripheral autonomic nervous system Is a False Autonomic neuropathy Inferred relationship Some
Benign neoplasm of autonomic nerve (disorder) Is a False Autonomic neuropathy Inferred relationship Some
Autonomic neuropathy due to amyloidosis Is a True Autonomic neuropathy Inferred relationship Some
Autonomic neuropathy due to diabetes mellitus (disorder) Is a False Autonomic neuropathy Inferred relationship Some
Segmental autonomic dysfunction Is a True Autonomic neuropathy Inferred relationship Some
Sphenopalatine neuralgia Is a True Autonomic neuropathy Inferred relationship Some
Pure autonomic failure (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Idiopathic diffuse hyperhidrosis Is a False Autonomic neuropathy Inferred relationship Some
Paraneoplastic autonomic dysfunction Is a True Autonomic neuropathy Inferred relationship Some
Superior laryngeal neuralgia Is a False Autonomic neuropathy Inferred relationship Some
Chronic idiopathic anhidrosis Is a False Autonomic neuropathy Inferred relationship Some
Vagus nerve laryngeal paralysis Is a False Autonomic neuropathy Inferred relationship Some
Drug-induced autonomic dysfunction Is a True Autonomic neuropathy Inferred relationship Some
Cauda equina syndrome with neurogenic urinary bladder Is a False Autonomic neuropathy Inferred relationship Some
An autosomal dominant disorder due to a sodium channelopathy and characterized by skin flushing and severe pain. Attacks can start in infancy where the pain is typically concentrated in the lower part of the body, with progression of age the location of pain may change to affect the head and face. Is a True Autonomic neuropathy Inferred relationship Some
Primary malignant nerve sheath neoplasm of autonomic nerve (disorder) Is a False Autonomic neuropathy Inferred relationship Some
Immature ganglionosis of large intestine (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Congenital hypoganglionosis of large intestine (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Autonomic neuropathy due to disorder of immune function (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Acquired hypoganglionosis of large intestine (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Autonomic neuropathy due to endocrine disease (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Autonomic neuropathy due to metabolic disease Is a True Autonomic neuropathy Inferred relationship Some
A rare, genetic, developmental defect during embryogenesis syndrome characterized by total or partial colonic aganglionosis associated with peripheral, usually multifocal, neuroblastic tumors (ganglioneuroblastoma, neuroblastoma, ganglioneuroma). Congenital central hypoventilation syndrome, with variable severity of respiratory compromise, cardiovascular and ophthalmologic symptoms, consistent with autonomic nervous system dysfunction, is occasionally associated. Is a True Autonomic neuropathy Inferred relationship Some
Autonomic neuropathy due to Refsum Disease Is a False Autonomic neuropathy Inferred relationship Some
Autonomic neuropathy due to Tangier disease (disorder) Is a False Autonomic neuropathy Inferred relationship Some
Autoimmune ganglionopathy Is a False Autonomic neuropathy Inferred relationship Some
Autonomic neuropathy due to medication induced hypoglycemia (disorder) Is a False Autonomic neuropathy Inferred relationship Some
Autonomic neuropathy due to Allgrove syndrome Is a False Autonomic neuropathy Inferred relationship Some
Autonomic neuropathy due to Fabry disease Is a False Autonomic neuropathy Inferred relationship Some
Autonomic ganglionopathy (disorder) Is a False Autonomic neuropathy Inferred relationship Some
Generalised diabetic autonomic neuropathy Is a False Autonomic neuropathy Inferred relationship Some
Hereditary autonomic neuropathy (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Neoplasm of autonomic nerve Is a True Autonomic neuropathy Inferred relationship Some
Aganglionosis of parasympathetic nerve ganglia Is a True Autonomic neuropathy Inferred relationship Some
Intestinal autonomic neuropathy Is a False Autonomic neuropathy Inferred relationship Some
Idiopathic peripheral autonomic neuropathy Is a True Autonomic neuropathy Inferred relationship Some
Paralysis of cervical sympathetic trunk (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Syndrome with characteristics of distal, slowly progressive muscular weakness, childhood-onset amyotrophy, autonomic dysfunction characterized by profuse sweating, distal cyanosis related to cold weather, orthostatic hypotension, and esophageal achalasia. It has been described in two sisters. Inheritance appears to be autosomal recessive. Is a True Autonomic neuropathy Inferred relationship Some
Amyotrophic lateral sclerosis with autonomic dysfunction (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Autoimmune disorder of autonomic nerve (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Familial visceral neuropathy Is a True Autonomic neuropathy Inferred relationship Some
Long segment Hirschsprung's disease Is a True Autonomic neuropathy Inferred relationship Some
Short segment Hirschsprung's disease Is a True Autonomic neuropathy Inferred relationship Some
Total intestinal aganglionosis Is a True Autonomic neuropathy Inferred relationship Some
Mowat-Wilson syndrome (disorder) Is a True Autonomic neuropathy Inferred relationship Some
A rare multiple congenital anomalies/dysmorphic syndrome characterized by Hirschsprung disease, facial dysmorphism (sloping forehead, high arched eyebrows, long eyelashes, telecanthus/hypertelorism, ptosis, prominent ears, thick earlobes, prominent nasal bridge, thick philtrum, everted lower lip vermillion and pointed chin), global developmental delay, intellectual disability and variable cerebral abnormalities (focal or generalized polymicrogyria, or hypoplastic corpus callosum). Is a True Autonomic neuropathy Inferred relationship Some
Haddad syndrome is a rare congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease. Is a True Autonomic neuropathy Inferred relationship Some
Hirschsprung disease-deafness-polydactyly syndrome is an extremely rare malformative association, described in only two siblings to date, characterized by Hirschsprung disease (defined by the presence of an aganglionic segment of variable extent in the terminal part of the colon that leads to symptoms of intestinal obstruction, including constipation and abdominal distension), polydactyly of hands and/or feet, unilateral renal agenesis, hypertelorism and congenital deafness. There have been no further descriptions in the literature since 1988. Is a True Autonomic neuropathy Inferred relationship Some
Hirschsprung disease of rectosigmoid region (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Extensive aganglionosis Hirschsprung disease (disorder) Is a True Autonomic neuropathy Inferred relationship Some
Waardenburg-Shah syndrome (WSS), also known as Waardenburg syndrome type 4 (WS4) is characterized by the association of Waardenburg syndrome (sensorineural hearing loss and pigmentary abnormalities) and Hirschsprung disease (aganglionic megacolon). Is a True Autonomic neuropathy Inferred relationship Some
Aganglionosis of Auerbach's plexus Is a True Autonomic neuropathy Inferred relationship Some

This concept is not in any reference sets

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