| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| X-linked distal arthrogryposis multiplex congenita (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
3 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2W |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Hereditary sensory and autonomic neuropathy type 8 (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
3 |
| PMP2-related Charcot-Marie-Tooth disease type 1 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
1 |
| Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
3 |
| Charcot-Marie-Tooth disease type 2T (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Autosomal recessive Charcot-Marie-Tooth disease type 2X |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
1 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2Z |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2Y |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Autosomal recessive intermediate Charcot-Marie-Tooth disease type D (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
1 |
| Charcot-Marie-Tooth disease type 2S |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2V (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
1 |
| Autosomal dominant Charcot-Marie-Tooth disease type 2DD |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| DNAJB2-related Charcot-Marie-Tooth disease type 2 |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
4 |
| Distal hereditary motor neuropathy type 5 (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Neurogenic scapuloperoneal syndrome Kaeser type (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
3 |
| Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
5 |
| Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
3 |
| Distal hereditary motor neuropathy type 2 (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
3 |
| Congenital insensitivity to pain with severe intellectual disability (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Congenital axonal neuropathy with encephalopathy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Hereditary sensory autonomic neuropathy type IIC |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Polyendocrine polyneuropathy syndrome (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Friedreich ataxia |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |
| Congenital insensitivity to pain, anosmia, neuropathic arthropathy |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
4 |
| Congenital insensitivity to pain, hyperhidrosis, absence of cutaneous sensory innervation (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
4 |
| Hereditary sensory and autonomic neuropathy type 6 (disorder) |
Finding site |
True |
Peripheral nervous system structure |
Inferred relationship |
Some |
2 |