Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Hereditary Motor and Sensory Neuropathy Type I
0 84 0 0 1 6.7E-03
Charcot-Marie-Tooth disease, demyelinating, Type 1F
0 6 0 0 2 2.8E-02
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder)
0 16 0 0 1 1.2E-02
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G
0 2 0 0 1 1.5E-02
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 3.0E-03 0 0
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal
109 0 1 2.3E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 3.1E-03 0 0
CUI: C0001127
Disease: Acidosis, Respiratory
Acidosis, Respiratory
13 0 1 3.0E-03 0 0
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris
94 0 1 2.4E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 2.9E-03 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly
138 0 1 2.2E-03 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases
9 0 1 3.0E-03 0 0
CUI: C0001622
Disease: Adrenal Gland Hyperfunction
Adrenal Gland Hyperfunction
50 0 1 2.7E-03 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia
87 0 1 2.5E-03 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related
89 0 1 2.4E-03 0 0
CUI: C0001818
Disease: Agoraphobia
Agoraphobia
29 0 1 2.9E-03 0 0
CUI: C0001889
Disease: Akinetic Mutism
Akinetic Mutism
1 0 1 3.1E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 2.7E-03 0 0
CUI: C0001957
Disease: Alcohol Withdrawal Delirium
Alcohol Withdrawal Delirium
23 0 1 2.9E-03 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria
13 0 1 3.0E-03 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia
86 0 1 2.5E-03 0 0
CUI: C0002351
Disease: Altitude Sickness
Altitude Sickness
10 0 1 3.0E-03 0 0
CUI: C0002382
Disease: Alveolar Bone Loss
Alveolar Bone Loss
101 0 1 2.4E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea
37 0 1 2.8E-03 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder
6 0 1 3.1E-03 0 0