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: C0162283
Disease: Nephrogenic Diabetes Insipidus
Nephrogenic Diabetes Insipidus 		60 41 12 0.17 24 0.40
CUI: C0677501
Disease: Congenital Nephrogenic Diabetes Insipidus
Congenital Nephrogenic Diabetes Insipidus 		11 0 5 0.17 0 0
CUI: C0267176
Disease: Gastroparesis with diabetes mellitus
Gastroparesis with diabetes mellitus 		21 0 5 0.12 0 0
CUI: C0268443
Disease: Acquired Nephrogenic Diabetes Insipidus
Acquired Nephrogenic Diabetes Insipidus 		3 0 3 0.12 0 0
CUI: C0472801
Disease: Hemophilia A carrier
Hemophilia A carrier 		3 0 3 0.12 0 0
CUI: C1563706
Disease: Nephrogenic Diabetes Insipidus, Type II
Nephrogenic Diabetes Insipidus, Type II 		3 24 3 0.12 8 0.14
CUI: C3542500
Disease: ADH-Resistant Diabetes Insipidus
ADH-Resistant Diabetes Insipidus 		3 0 3 0.12 0 0
CUI: C1845202
Disease: Nephrogenic Syndrome of Inappropriate Antidiuresis
Nephrogenic Syndrome of Inappropriate Antidiuresis 		14 4 4 0.12 1 2.2E-02
CUI: C4728047
Disease: Left anterior descending coronary artery occlusion
Left anterior descending coronary artery occlusion 		5 0 3 0.12 0 0
CUI: C0270985
Disease: Alcohol myopathy
Alcohol myopathy 		6 0 3 0.11 0 0
CUI: C1370868
Disease: Refractory Chronic Myelogenous Leukemia, BCR-ABL1 Positive
Refractory Chronic Myelogenous Leukemia, BCR-ABL1 Positive 		6 0 3 0.11 0 0
CUI: C3888004
Disease: HERMANSKY-PUDLAK SYNDROME 5
HERMANSKY-PUDLAK SYNDROME 5 		6 0 3 0.11 0 0
CUI: C0018425
Disease: Gyrate Atrophy
Gyrate Atrophy 		8 0 3 0.10 0 0
CUI: C1135188
Disease: Critical illness myopathy
Critical illness myopathy 		8 0 3 0.10 0 0
CUI: C0476237
Disease: Metabolic symptoms
Metabolic symptoms 		9 0 3 1.0E-01 0 0
CUI: C0546483
Disease: Lung cyst
Lung cyst 		9 0 3 1.0E-01 0 0
CUI: C1737261
Disease: Acute myeloid leukaemia progression
Acute myeloid leukaemia progression 		9 0 3 1.0E-01 0 0
CUI: C0272324
Disease: Mild hereditary factor VIII deficiency disease
Mild hereditary factor VIII deficiency disease 		11 0 3 9.4E-02 0 0
CUI: C0751699
Disease: Minimally Conscious State
Minimally Conscious State 		12 0 3 9.1E-02 0 0
CUI: C0021141
Disease: Inappropriate ADH Syndrome
Inappropriate ADH Syndrome 		14 0 3 8.6E-02 0 0
CUI: C0003546
Disease: Aphasia, Acquired
Aphasia, Acquired 		2 0 2 8.3E-02 0 0
CUI: C0234462
Disease: Aphasia, Ageusic
Aphasia, Ageusic 		2 0 2 8.3E-02 0 0
CUI: C0234469
Disease: Aphasia, Global
Aphasia, Global 		2 0 2 8.3E-02 0 0
CUI: C0234472
Disease: Aphasia, Functional
Aphasia, Functional 		2 0 2 8.3E-02 0 0
CUI: C0234474
Disease: Aphasia, Graphomotor
Aphasia, Graphomotor 		2 0 2 8.3E-02 0 0