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 |
|