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: C0040416
Disease: Tonic Pupil
Tonic Pupil
1 0 1 4.8E-02 0 0
CUI: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease
1 0 1 4.8E-02 0 0
CUI: C0751059
Disease: Cranial Neuropathies, Multiple
Cranial Neuropathies, Multiple
1 0 1 4.8E-02 0 0
CUI: C0795865
Disease: Chromosome 17, trisomy 17p
Chromosome 17, trisomy 17p
1 0 1 4.8E-02 0 0
ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION
1 0 1 4.8E-02 0 0
CUI: C0850629
Disease: radiating back pain
radiating back pain
1 0 1 4.8E-02 0 0
CUI: C1695985
Disease: Lewis-Sumner syndrome
Lewis-Sumner syndrome
1 0 1 4.8E-02 0 0
CUI: C1838818
Disease: MUSCLE STIFFNESS, PAINFUL
MUSCLE STIFFNESS, PAINFUL
1 0 1 4.8E-02 0 0
CUI: C1838868
Disease: Corticospinal tract atrophy
Corticospinal tract atrophy
1 0 1 4.8E-02 0 0
ATAXIA AND POLYNEUROPATHY, ADULT-ONSET
1 0 1 4.8E-02 0 0
STRIATAL NECROSIS, BILATERAL, WITH DYSTONIA
1 0 1 4.8E-02 0 0
Striatonigral Degeneration, Infantile, Mitochondrial
1 0 1 4.8E-02 0 0
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5
1 0 1 4.8E-02 0 0
Nonsyndromic sensorineural hearing loss
1 0 1 4.8E-02 0 0
Charcot-Marie-Tooth Disease, Dominant Intermediate D
1 0 1 4.8E-02 0 0
Charcot-Marie-Tooth disease, Type 2J
1 0 1 4.8E-02 0 0
Charcot-Marie-Tooth disease, demyelinating, Type 1F
1 0 1 4.8E-02 0 0
CUI: C1843169
Disease: Clusters of axonal regeneration
Clusters of axonal regeneration
1 0 1 4.8E-02 0 0
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder)
1 0 1 4.8E-02 0 0
Charcot-Marie-Tooth disease, Type 1D (disorder)
1 0 1 4.8E-02 0 0
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder)
1 0 1 4.8E-02 0 0
Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma
1 0 1 4.8E-02 0 0
Charcot-Marie-Tooth Neuropathy, Type 4B2, with Early-Onset Glaucoma
1 0 1 4.8E-02 0 0
Charcot-Marie-Tooth disease and deafness
1 0 1 4.8E-02 0 0
Charcot-Marie-Tooth disease, Type 1E
1 0 1 4.8E-02 0 0