Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C1854454
Disease: Axonal regeneration
Axonal regeneration 		5 0 1 0.12 0 0
CUI: C0235857
Disease: Decreased lacrimation
Decreased lacrimation 		6 1 1 0.11 1 0.50
CUI: C1832776
Disease: Hypertrophic nerve changes
Hypertrophic nerve changes 		6 0 1 0.11 0 0
CUI: C0393807
Disease: Hereditary motor and sensory neuropathy with optic atrophy (disorder)
Hereditary motor and sensory neuropathy with optic atrophy (disorder) 		7 0 1 1.0E-01 0 0
CUI: C1328349
Disease: Neuropathy ataxia and retinis pigmentosa
Neuropathy ataxia and retinis pigmentosa 		7 0 1 1.0E-01 0 0
CUI: C2079538
Disease: Charcot-Marie-Tooth disease, Type 2A
Charcot-Marie-Tooth disease, Type 2A 		7 0 1 1.0E-01 0 0
CUI: C4024927
Disease: Peripheral hypomyelination
Peripheral hypomyelination 		7 0 1 1.0E-01 0 0
CUI: C4721916
Disease: HMSN Type V
HMSN Type V 		7 0 1 1.0E-01 0 0
CUI: C1262113
Disease: Lipohypertrophy
Lipohypertrophy 		8 0 1 9.1E-02 0 0
CUI: C1968790
Disease: Axonal degeneration/regeneration
Axonal degeneration/regeneration 		8 0 2 0.20 0 0
CUI: C2751584
Disease: Neurodegeneration Due To Cerebral Folate Transport Deficiency
Neurodegeneration Due To Cerebral Folate Transport Deficiency 		8 5 1 9.1E-02 1 0.17
CUI: C4021222
Disease: Impaired temperature sensation
Impaired temperature sensation 		8 0 1 9.1E-02 0 0
CUI: C0392553
Disease: Hereditary peripheral neuropathy
Hereditary peripheral neuropathy 		9 0 1 8.3E-02 0 0
CUI: C0393907
Disease: Axonal sensorimotor neuropathy
Axonal sensorimotor neuropathy 		9 0 1 8.3E-02 0 0
CUI: C1836527
Disease: Distal sensory impairment of all modalities
Distal sensory impairment of all modalities 		9 0 1 8.3E-02 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw 		9 0 1 8.3E-02 0 0
CUI: C4025830
Disease: Peripheral axonal degeneration
Peripheral axonal degeneration 		9 0 1 8.3E-02 0 0
CUI: C0239377
Disease: Arm Pain
Arm Pain 		10 0 1 7.7E-02 0 0
CUI: C0239830
Disease: Hand muscle atrophy
Hand muscle atrophy 		10 0 1 7.7E-02 0 0
CUI: C0279746
Disease: Adenocarcinoma of salivary gland
Adenocarcinoma of salivary gland 		10 0 1 7.7E-02 0 0
CUI: C0751576
Disease: Partial Paralysis (Paresis) Vocal Cords
Partial Paralysis (Paresis) Vocal Cords 		10 0 2 0.17 0 0
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome 		10 0 1 7.7E-02 0 0
CUI: C1851085
Disease: Severe expressive language delay
Severe expressive language delay 		11 0 1 7.1E-02 0 0
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3 		12 0 1 6.7E-02 0 0
CUI: C0852262
Disease: Placental abnormalities (excl neoplasms)
Placental abnormalities (excl neoplasms) 		12 0 1 6.7E-02 0 0