| 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 | 
| Huntington's chorea with hyperactive behavior (disorder) | 
Finding site | 
True | 
Peripheral nervous system structure | 
Inferred relationship | 
Some | 
 4 |