Source: UNIPROT ×
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: C1855772
Disease: Absent corpus callosum cataract immunodeficiency
Absent corpus callosum cataract immunodeficiency 		1 0 1 1.7E-03 0 0
CUI: C0338106
Disease: Adenocarcinoma of colon
Adenocarcinoma of colon 		2 0 1 1.7E-03 0 0
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		54 0 1 1.6E-03 0 0
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		54 0 4 6.4E-03 0 0
CUI: C0206686
Disease: Adrenocortical carcinoma
Adrenocortical carcinoma 		1 0 1 1.7E-03 0 0
CUI: C3807327
Disease: ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1
ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1 		1 0 1 1.7E-03 0 0
CUI: C3808874
Disease: ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2
ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2 		1 0 1 1.7E-03 0 0
CUI: C3539013
Disease: AICARDI-GOUTIERES SYNDROME 6
AICARDI-GOUTIERES SYNDROME 6 		1 0 1 1.7E-03 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		3 0 1 1.7E-03 0 0
CUI: C1835922
Disease: Aminoacylase 1 deficiency
Aminoacylase 1 deficiency 		1 0 1 1.7E-03 0 0
CUI: C1842675
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) 		1 0 1 1.7E-03 0 0
CUI: C4479357
Disease: ANAUXETIC DYSPLASIA 2
ANAUXETIC DYSPLASIA 2 		1 0 1 1.7E-03 0 0
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome 		1 0 1 1.7E-03 0 0
CUI: C2936791
Disease: Antley-Bixler Syndrome, Autosomal Dominant
Antley-Bixler Syndrome, Autosomal Dominant 		1 0 1 1.7E-03 0 0
CUI: C4015368
Disease: AORTIC ANEURYSM, FAMILIAL THORACIC 9
AORTIC ANEURYSM, FAMILIAL THORACIC 9 		1 0 1 1.7E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		1 0 1 1.7E-03 0 0
CUI: C0268547
Disease: Argininosuccinic Aciduria
Argininosuccinic Aciduria 		1 0 1 1.7E-03 0 0
CUI: C0796028
Disease: ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION
ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION 		1 0 1 1.7E-03 0 0
CUI: C4012790
Disease: Ataxia-Telangiectasisa-Like Disorder 1
Ataxia-Telangiectasisa-Like Disorder 1 		1 0 1 1.7E-03 0 0
CUI: C3668942
Disease: Atelosteogenesis Type 3
Atelosteogenesis Type 3 		1 0 1 1.7E-03 0 0
CUI: C0265283
Disease: Atelosteogenesis, type 1
Atelosteogenesis, type 1 		1 0 1 1.7E-03 0 0
CUI: C2751315
Disease: Atrial Septal Defect 6
Atrial Septal Defect 6 		1 0 1 1.7E-03 0 0
CUI: C1840333
Disease: Barakat syndrome
Barakat syndrome 		1 0 1 1.7E-03 0 0
CUI: C1855849
Disease: Bartter syndrome, antenatal , type 2
Bartter syndrome, antenatal , type 2 		1 0 1 1.7E-03 0 0
CUI: C4310820
Disease: BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT
BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT 		1 0 1 1.7E-03 0 0