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 |