| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| X-linked distal arthrogryposis multiplex congenita |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2W |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary sensory and autonomic neuropathy type 8 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Charcot-Marie-Tooth disease type 2T |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive Charcot-Marie-Tooth disease type 2X |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2Z |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2Y |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2 due to trafficking from endoplasmic reticulum to golgi regulator mutation |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive intermediate Charcot-Marie-Tooth disease type D |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 2S |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2V |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2DD |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| DnaJ heat shock protein family (Hsp40) member B2-related Charcot-Marie-Tooth disease type 2 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
4 |
| Distal hereditary motor neuropathy type 5 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Neurogenic scapuloperoneal syndrome Kaeser type |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
5 |
| Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Distal hereditary motor neuropathy type 2 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Congenital insensitivity to pain with severe intellectual disability |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital axonal neuropathy with encephalopathy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary sensory autonomic neuropathy type IIC |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Polyendocrine polyneuropathy syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| [X]Polyneuropathy in neoplastic disease classified elsewhere |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| [X]Other mononeuropathies in diseases classified elsewhere |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| [X]Polyneuropathy in nutritional deficiency classified elsewhere |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| [X]Other specified mononeuropathies |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Disorder of muscle tone of newborn |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
2 |
| Other specified disorders of peripheral nervous system |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Peripheral nervous system disorder NOS |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Trigeminal neuralgia [no drugs here] |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Neuralgia, neuritis and radiculitis unspecified |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Neuralgia unspecified |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Radiculitis unspecified |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Mononeuritis of unspecified site NOS |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Other idiopathic peripheral neuropathy |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Other idiopathic peripheral neuropathy NOS |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Peroneal muscular atrophy NOS |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Neuralgia, neuritis or radiculitis NOS |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Trigeminal neuralgia NOS |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Other specified trigeminal neuralgia |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Hereditary peripheral neuropathy NOS |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Algoneurodystrophy NOS |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Disorder of muscle tone of newborn |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
3 |
| Symptomatic diabetic peripheral neuropathy |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|
| Disorder of muscle tone of newborn |
Finding site |
False |
Peripheral nervous system structure |
Inferred relationship |
Existential restriction modifier |
|