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: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 1 9.1E-04 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 3.9E-03 0 0
CUI: C0000846
Disease: Agenesis
Agenesis 		161 0 1 6.1E-03 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans 		64 0 1 1.5E-02 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 1 2.0E-02 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		52 0 1 1.8E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 1 4.2E-02 0 0
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		2235 0 2 8.9E-04 0 0
CUI: C0001430
Disease: Adenoma
Adenoma 		1183 0 2 1.7E-03 0 0
CUI: C0001622
Disease: Adrenal Gland Hyperfunction
Adrenal Gland Hyperfunction 		50 0 1 1.9E-02 0 0
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		90 0 2 2.2E-02 0 0
CUI: C0001624
Disease: Adrenal Gland Neoplasms
Adrenal Gland Neoplasms 		94 0 1 1.0E-02 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		87 0 2 2.2E-02 0 0
CUI: C0001787
Disease: Osteoporosis, Age-Related
Osteoporosis, Age-Related 		89 0 1 1.1E-02 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria 		76 0 1 1.3E-02 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		3397 0 2 5.9E-04 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 1.1E-02 0 0
CUI: C0002438
Disease: Amebiasis
Amebiasis 		37 0 1 2.4E-02 0 0
CUI: C0002448
Disease: Ameloblastoma
Ameloblastoma 		174 0 1 5.6E-03 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		37 0 1 2.4E-02 0 0
CUI: C0002726
Disease: Amyloidosis
Amyloidosis 		694 0 1 1.4E-03 0 0
CUI: C0003090
Disease: Ankylosis
Ankylosis 		15 0 1 5.3E-02 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate 		139 0 1 7.0E-03 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		102 0 2 1.9E-02 0 0
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation 		53 0 2 3.6E-02 0 0