| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Hereditary sensory and autonomic neuropathy with spastic paraplegia |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
4 |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type E |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Primary malignant nerve sheath neoplasm of peripheral nervous system structure |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Metastatic malignant neoplasm of peripheral nervous system |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive Charcot-Marie-Tooth disease with hoarseness |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 2B1 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Spastic paraplegia, optic atrophy, neuropathy syndrome |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
4 |
| Ataxia co-occurrent and due to phytanic acid storage disease |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
4 |
| Complex regional pain syndrome, type II |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Complex regional pain syndrome type I |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4A |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4C |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4D |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4G |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4B2 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4F |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4H |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4B1 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4J |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4E |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 4B3 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| X-linked Charcot-Marie-Tooth disease type 6 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| X-linked hereditary motor and sensory neuropathy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| X-linked Charcot-Marie-Tooth disease type 4 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| X-linked Charcot-Marie-Tooth disease type 1 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| X-linked Charcot-Marie-Tooth disease type 2 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| X-linked Charcot-Marie-Tooth disease type 3 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| X-linked Charcot-Marie-Tooth disease type 5 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Microcephalus, complex motor and sensory axonal neuropathy syndrome |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2A2 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant slowed nerve conduction velocity |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2U |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type A |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type B |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type C |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type D |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Severe early-onset axonal neuropathy due to mitofusin 2 deficiency |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type F |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Hereditary motor and sensory neuropathy type 5 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary motor and sensory neuropathy with acrodystrophy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Charcot-Marie-Tooth disease type 2B5 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Cervical hypertrichosis and peripheral neuropathy syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type A |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type C |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type D |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease type B |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive intermediate Charcot-Marie-Tooth disease type A |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive intermediate Charcot-Marie-Tooth disease type B |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive intermediate Charcot-Marie-Tooth disease type C |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2Q |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Charcot-Marie-Tooth disease type 2R |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Periodic paralysis with transient compartment-like syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Periodic paralysis with later-onset distal motor neuropathy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2O |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Infectious disorder of the peripheral nervous system |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Hereditary sensory and autonomic neuropathy due to tectonin beta-propeller repeat containing 2 mutation |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
4 |
| Childhood-onset autosomal recessive myopathy with external ophthalmoplegia |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary sensory and autonomic neuropathy type 7 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Charcot-Marie-Tooth disease type 2P |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary sensorimotor neuropathy with hyperelastic skin |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Schwartz-Jampel syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Roussy-Lévy syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Hereditary autonomic neuropathy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary sensory autonomic neuropathy type IIA |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary sensory autonomic neuropathy type IIB |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary sensory autonomic neuropathy type ID |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary sensory autonomic neuropathy type IE |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary sensory autonomic neuropathy type IA |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary sensory autonomic neuropathy type IC |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Huntington's chorea |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
5 |
| Juvenile onset Huntington's disease |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
4 |
| Late onset Huntington's disease |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
4 |
| Akinetic-rigid form of Huntington's disease |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
4 |
| Hypertrophic interstitial neuropathy |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Déjérine-Sottas disease |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Neonatal hypotonia |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Neonatal neuromuscular disorder |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Microcephalus, complex motor and sensory axonal neuropathy syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal recessive Charcot-Marie-Tooth disease type 2 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive distal hereditary motor neuropathy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant distal hereditary motor neuropathy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| X-linked distal hereditary motor neuropathy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive distal spinal muscular atrophy type 3 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Distal hereditary motor neuropathy Jerash type |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Young adult-onset distal hereditary motor neuropathy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Spinal muscular atrophy with respiratory distress type 1 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant spastic paraplegia type 17 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Distal hereditary motor neuropathy type 1 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Distal hereditary motor neuropathy type 7 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal dominant congenital benign spinal muscular atrophy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
4 |
| Spinal muscular atrophy with respiratory distress type 2 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| X-linked distal spinal muscular atrophy type 3 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| X-linked distal arthrogryposis multiplex congenita |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |