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53520000: Autonomic nerve structure (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
198452010 Peripheral autonomic nerve en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
496688019 Autonomic nerve structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
791649013 Autonomic nerve structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2818671000005112 Autonom nervestruktur da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


289 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autonomic nerve structure Is a Autonomic nervous system structure true Inferred relationship Some
Autonomic nerve structure Is a Peripheral nerve structure false Inferred relationship Some
Autonomic nerve structure del af Entire autonomic nervous system false Additional relationship Some
Autonomic nerve structure del af Entire peripheral nervous system false Additional relationship Some
Autonomic nerve structure Is a Structure of peripheral part of autonomic nervous system (body structure) false Inferred relationship Some
Autonomic nerve structure Is a Nerve structure true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Autonomic disorder involving unilateral hyperhydrosis and flushing of the head and neck. Finding site True Autonomic nerve structure Inferred relationship Some 2
Autonomic neuropathy due to type 1 diabetes mellitus (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 2
Autonomic neuropathy due to type 2 diabetes mellitus (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 2
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). Finding site True Autonomic nerve structure Inferred relationship Some 5
Haddad syndrome is a rare congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease. Finding site True Autonomic nerve structure Inferred relationship Some 3
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). Finding site True Autonomic nerve structure Inferred relationship Some 6
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. Finding site True Autonomic nerve structure Inferred relationship Some 4
Hirschsprung disease-type D brachydactyly syndrome is characterized by Hirschsprung disease and absence or hypoplasia of the nails and distal phalanges of the thumbs and great toes (type D brachydactyly). It has been described in four males from one family (two brothers and two maternal uncles). Transmission appears to be X-linked recessive but autosomal dominant inheritance with incomplete penetrance in females cannot be ruled out. Finding site True Autonomic nerve structure Inferred relationship Some 4
Hirschsprung disease-nail hypoplasia-dysmorphism syndrome is a fatal malformative disorder that is characterised by Hirschsprung disease, hypoplastic nails, distal limb hypoplasia and minor craniofacial dysmorphic features (flat facies, upward slanting palpebral fissures, narrow philtrum, narrow, high arched palate, micrognathia, low set ears with abnormal helices). Hydronephrosis has also been reported. There have been no further descriptions in the literature since 1988. Finding site True Autonomic nerve structure Inferred relationship Some 5
Acquired Horner syndrome (disorder) Finding site False Autonomic nerve structure Inferred relationship Some 2
Primary malignant nerve sheath neoplasm of autonomic nerve (disorder) Finding site False Autonomic nerve structure Inferred relationship Some 2
Primary malignant nerve sheath neoplasm of autonomic nerve (disorder) Finding site False Autonomic nerve structure Inferred relationship Some 3
Hirschsprung disease of rectosigmoid region (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 3
Extensive aganglionosis Hirschsprung disease (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 3
Autonomic neuropathy due to disorder of immune function (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 1
Auriculotemporal syndrome of right auriculotemporal nerve (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 4
Auriculotemporal syndrome of left auriculotemporal nerve (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 4
Autonomic neuropathy due to endocrine disease (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 1
Autonomic neuropathy due to metabolic disease Finding site True Autonomic nerve structure Inferred relationship Some 1
Diarrhea due to diabetes mellitus Finding site True Autonomic nerve structure Inferred relationship Some 4
Gastroparesis due to type 1 diabetes mellitus Finding site True Autonomic nerve structure Inferred relationship Some 2
Gastroparesis due to type 2 diabetes mellitus (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 2
Gastroparesis due to diabetes mellitus (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 2
Congenital Horner syndrome is a rare neurological disorder characterized by relative pupillary miosis and blepharoptosis, evident at birth, caused by interruption of the oculosympathetic innervation at any point along the neural pathway from the hypothalamus to the orbit. Often additional symptoms, such as enophthalmos, facial anhidrosis, iris heterochromia, conjunctival congestion, transient hypotonia and/or pupillary dilation lag, may be present. Association with birth trauma, neoplasms or vascular malformations has been reported. Finding site False Autonomic nerve structure Inferred relationship Some 2
Right cervical sympathetic dystrophy Finding site False Autonomic nerve structure Inferred relationship Some 2
Left cervical sympathetic dystrophy Finding site False Autonomic nerve structure Inferred relationship Some 2
Aganglionosis of large intestine (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 2
A rare genetic developmental defect during embryogenesis syndrome with characteristics of total or partial colonic aganglionosis associated with peripheral usually multifocal, neuroblastic neoplasm (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. Finding site True Autonomic nerve structure Inferred relationship Some 4
Long segment Hirschsprung's disease Finding site True Autonomic nerve structure Inferred relationship Some 2
Short segment Hirschsprung's disease Finding site True Autonomic nerve structure Inferred relationship Some 2
Post-ganglionic parasympathetic nerves that facilitate penile erection. Is a True Autonomic nerve structure Inferred relationship Some
Acquired Horner syndrome (disorder) Finding site False Autonomic nerve structure Inferred relationship Some 1
Acquired right-sided Horner syndrome (disorder) Finding site False Autonomic nerve structure Inferred relationship Some 1
Acquired left-sided Horner syndrome (disorder) Finding site False Autonomic nerve structure Inferred relationship Some 1
Autonomic neuropathy due to Refsum Disease Finding site True Autonomic nerve structure Inferred relationship Some 1
Autonomic neuropathy due to Tangier disease (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 1
Autonomic neuropathy due to medication induced hypoglycemia (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 1
Autonomic neuropathy due to Allgrove syndrome Finding site True Autonomic nerve structure Inferred relationship Some 1
Autonomic neuropathy due to Fabry disease Finding site True Autonomic nerve structure Inferred relationship Some 1
Generalised diabetic autonomic neuropathy Finding site True Autonomic nerve structure Inferred relationship Some 1
Hereditary autonomic neuropathy (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 1
Malignant nerve sheath neoplasm of overlapping sites of peripheral nerves and autonomic nervous system (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 1
Mowat-Wilson syndrome due to monosomy 2q22 (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 4
Autonomic neuropathy due to drug induced diabetes mellitus Finding site True Autonomic nerve structure Inferred relationship Some 1
Peripheral autonomic neuropathy due to diabetes mellitus (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 2
Parkinsonian syndrome with idiopathic orthostatic hypotension (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 4
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. Finding site True Autonomic nerve structure Inferred relationship Some 1
Primary malignant nerve sheath neoplasm of autonomic nerve (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 1
Amyotrophic lateral sclerosis with autonomic dysfunction (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 1
Disorder of autonomic nerve due to Guillain-Barre Syndrome (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 1
Disorder of autonomic nerve due to impaired glucose tolerance (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 1
Autoimmune disorder of autonomic nerve (disorder) Finding site True Autonomic nerve structure Inferred relationship Some 1
Autonomic neuropathy due to multiple endocrine neoplasia type 2b Finding site True Autonomic nerve structure Inferred relationship Some 1
Limited autoimmune autonomic neuropathy Finding site True Autonomic nerve structure Inferred relationship Some 1
Neurolytic autonomic nerve block Procedure site - Indirect (attribute) True Autonomic nerve structure Inferred relationship Some 1
Intravenous regional autonomic block Procedure site True Autonomic nerve structure Inferred relationship Some 1

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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