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: C4016716
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, AUTOSOMAL RECESSIVE
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, AUTOSOMAL RECESSIVE 		1 0 1 4.8E-02 0 0
CUI: C4016717
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, WITH FOCALLY FOLDED MYELIN SHEATHS
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, WITH FOCALLY FOLDED MYELIN SHEATHS 		1 0 1 4.8E-02 0 0
CUI: C4016973
Disease: NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE
NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE 		1 0 1 4.8E-02 0 0
CUI: C4020736
Disease: Elevated urinary homovanillic acid
Elevated urinary homovanillic acid 		1 0 1 4.8E-02 0 0
CUI: C4020904
Disease: Myelin tomacula
Myelin tomacula 		1 0 1 4.8E-02 0 0
CUI: C4021684
Disease: Sclerosis of hand bone
Sclerosis of hand bone 		1 0 1 4.8E-02 0 0
CUI: C4022125
Disease: Aplasia of the phalanges of the 3rd toe
Aplasia of the phalanges of the 3rd toe 		1 0 1 4.8E-02 0 0
CUI: C4022667
Disease: Small toe
Small toe 		1 0 1 4.8E-02 0 0
CUI: C4023222
Disease: Abnormal electrophysiology of sinoatrial node origin
Abnormal electrophysiology of sinoatrial node origin 		1 0 1 4.8E-02 0 0
CUI: C4023690
Disease: Spontaneous pain sensation
Spontaneous pain sensation 		1 0 1 4.8E-02 0 0
CUI: C4024922
Disease: Irregular myelin loops
Irregular myelin loops 		1 0 1 4.8E-02 0 0
CUI: C4024933
Disease: Acute demyelinating polyneuropathy
Acute demyelinating polyneuropathy 		1 0 1 4.8E-02 0 0
CUI: C4024938
Disease: Segmental peripheral demyelination
Segmental peripheral demyelination 		1 0 1 4.8E-02 0 0
CUI: C4024964
Disease: Intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material
Intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material 		1 0 1 4.8E-02 0 0
CUI: C4025322
Disease: Prolonged brainstem auditory evoked potentials
Prolonged brainstem auditory evoked potentials 		1 0 1 4.8E-02 0 0
CUI: C4025339
Disease: Abnormality of circulating leptin level
Abnormality of circulating leptin level 		1 0 1 4.8E-02 0 0
CUI: C4025868
Disease: Increased facial adipose tissue
Increased facial adipose tissue 		1 0 1 4.8E-02 0 0
CUI: C4229131
Disease: Distal acroosteolysis
Distal acroosteolysis 		1 0 1 4.8E-02 0 0
CUI: C4310725
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B 		1 0 1 4.8E-02 0 0
CUI: C4310875
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2A
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2A 		1 0 1 4.8E-02 0 0
CUI: C4531142
Disease: Abnormal lymphocyte physiology
Abnormal lymphocyte physiology 		1 0 1 4.8E-02 0 0
CUI: C4538604
Disease: Alpha-aminoadipic aciduria
Alpha-aminoadipic aciduria 		1 0 1 4.8E-02 0 0
CUI: C4693509
Disease: CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G 		1 0 1 4.8E-02 0 0
CUI: C4706465
Disease: X-linked Charcot-Marie-Tooth disease type 1
X-linked Charcot-Marie-Tooth disease type 1 		1 0 1 4.8E-02 0 0
CUI: C4707897
Disease: Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
Severe early-onset axonal neuropathy due to mitofusin 2 deficiency 		1 0 1 4.8E-02 0 0