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: C0018523
Disease: Hallervorden-Spatz Syndrome
Hallervorden-Spatz Syndrome 		0 42 0 0 1 2.1E-02
CUI: C1849452
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder) 		0 13 0 0 1 5.3E-02
CUI: C0000729
Disease: Abdominal Cramps
Abdominal Cramps 		1 0 1 5.5E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 1 4.0E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		11 0 1 5.2E-03 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans 		64 0 1 4.1E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 1 4.4E-03 0 0
CUI: C0001122
Disease: Acidosis
Acidosis 		28 0 1 4.8E-03 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis 		3 0 1 5.4E-03 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 0 1 3.1E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 5.2E-03 0 0
CUI: C0001306
Disease: Acute alcoholic liver disease
Acute alcoholic liver disease 		35 0 1 4.6E-03 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease 		111 0 1 3.4E-03 0 0
CUI: C0001420
Disease: Papillary adenocarcinoma
Papillary adenocarcinoma 		11 0 1 5.2E-03 0 0
CUI: C0001614
Disease: Adrenal Cortex Diseases
Adrenal Cortex Diseases 		13 0 1 5.1E-03 0 0
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms 		23 0 1 4.9E-03 0 0
CUI: C0001825
Disease: Agraphia
Agraphia 		3 0 1 5.4E-03 0 0
CUI: C0001857
Disease: AIDS related complex
AIDS related complex 		100 0 1 3.5E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 1 4.4E-03 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria 		76 0 1 3.9E-03 0 0
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		218 0 1 2.5E-03 0 0
CUI: C0002103
Disease: Atopic rhinitis
Atopic rhinitis 		13 0 1 5.1E-03 0 0
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		114 0 1 3.4E-03 0 0
CUI: C0002382
Disease: Alveolar Bone Loss
Alveolar Bone Loss 		101 0 1 3.5E-03 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 5.0E-03 0 0