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: C0596992
Disease: myelinopathy
myelinopathy
3 0 2 0.50 0 0
CUI: C0422879
Disease: CNS symptom
CNS symptom
1 0 1 0.33 0 0
CUI: C0751059
Disease: Cranial Neuropathies, Multiple
Cranial Neuropathies, Multiple
1 0 1 0.33 0 0
CUI: C0795865
Disease: Chromosome 17, trisomy 17p
Chromosome 17, trisomy 17p
1 0 1 0.33 0 0
CUI: C1695985
Disease: Lewis-Sumner syndrome
Lewis-Sumner syndrome
1 0 1 0.33 0 0
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3 (disorder)
1 0 1 0.33 0 0
Charcot-Marie-Tooth disease and deafness
1 0 1 0.33 0 0
Charcot-Marie-Tooth disease, Type 1E
1 0 1 0.33 0 0
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e
1 0 1 0.33 0 0
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, AUTOSOMAL RECESSIVE
1 0 1 0.33 0 0
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, WITH FOCALLY FOLDED MYELIN SHEATHS
1 0 1 0.33 0 0
CUI: C4020904
Disease: Myelin tomacula
Myelin tomacula
1 0 1 0.33 0 0
CUI: C4023690
Disease: Spontaneous pain sensation
Spontaneous pain sensation
1 0 1 0.33 0 0
CUI: C4024933
Disease: Acute demyelinating polyneuropathy
Acute demyelinating polyneuropathy
1 0 1 0.33 0 0
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29
1 0 1 0.33 0 0
X-linked Charcot-Marie-Tooth disease type 1
1 0 1 0.33 0 0
CUI: C0016579
Disease: Formication
Formication
2 0 1 0.25 0 0
CUI: C0235044
Disease: Paresthesia, Distal
Paresthesia, Distal
2 0 1 0.25 0 0
CUI: C0262576
Disease: Nerve paralysis
Nerve paralysis
2 0 1 0.25 0 0
CUI: C0474520
Disease: Myokymia, Generalized
Myokymia, Generalized
2 0 1 0.25 0 0
CUI: C0751412
Disease: Painful Paresthesias
Painful Paresthesias
2 0 1 0.25 0 0
CUI: C0751460
Disease: Flaccid Quadriplegia
Flaccid Quadriplegia
2 0 1 0.25 0 0
CUI: C0751461
Disease: Paralysis, Spinal, Quadriplegic
Paralysis, Spinal, Quadriplegic
2 0 1 0.25 0 0
CUI: C0751922
Disease: Median Neuropathy
Median Neuropathy
2 0 1 0.25 0 0
CUI: C1290871
Disease: Disorder of hand
Disorder of hand
2 0 1 0.25 0 0