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: C0268435
Disease: Renal Tubular Acidosis, Type II
Renal Tubular Acidosis, Type II 		13 0 2 4.8E-02 0 0
CUI: C1704380
Disease: Distal Renal Tubular Acidosis
Distal Renal Tubular Acidosis 		23 0 2 3.8E-02 0 0
CUI: C1533041
Disease: Primary congenital glaucoma
Primary congenital glaucoma 		24 0 2 3.8E-02 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis 		25 0 2 3.7E-02 0 0
CUI: C0865800
Disease: asthma with copd
asthma with copd 		29 0 2 3.4E-02 0 0
CUI: C0278252
Disease: Prognosis bad
Prognosis bad 		1 0 1 3.2E-02 0 0
CUI: C0339512
Disease: Bull's eye macular dystrophy
Bull's eye macular dystrophy 		1 0 1 3.2E-02 0 0
CUI: C0599909
Disease: stress related disorder
stress related disorder 		1 0 1 3.2E-02 0 0
CUI: C1334557
Disease: Malignant Adult Brain Neoplasm
Malignant Adult Brain Neoplasm 		1 0 1 3.2E-02 0 0
CUI: C1513718
Disease: Mucin-Producing Intrahepatic Cholangiocarcinoma
Mucin-Producing Intrahepatic Cholangiocarcinoma 		1 0 1 3.2E-02 0 0
CUI: C1836027
Disease: Deafness, Autosomal Recessive 23
Deafness, Autosomal Recessive 23 		1 0 1 3.2E-02 0 0
CUI: C1836336
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H 		1 0 1 3.2E-02 0 0
CUI: C1850318
Disease: Omodysplasia type 1
Omodysplasia type 1 		1 0 1 3.2E-02 0 0
CUI: C1851120
Disease: Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia
Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia 		1 0 1 3.2E-02 0 0
CUI: C1854990
Disease: Molybdenum Cofactor Deficiency, Complementation Group C
Molybdenum Cofactor Deficiency, Complementation Group C 		1 0 1 3.2E-02 0 0
CUI: C1858626
Disease: Bicarbonate-wasting renal tubular acidosis
Bicarbonate-wasting renal tubular acidosis 		1 0 1 3.2E-02 0 0
CUI: C1858628
Disease: Increased red cell osmotic resistance
Increased red cell osmotic resistance 		1 0 1 3.2E-02 0 0
CUI: C1865885
Disease: Usher Syndrome, Type IF
Usher Syndrome, Type IF 		1 0 1 3.2E-02 0 0
CUI: C1968610
Disease: Anterolateral radial head dislocation
Anterolateral radial head dislocation 		1 0 1 3.2E-02 0 0
CUI: C1970309
Disease: Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation 		1 0 1 3.2E-02 0 0
CUI: C2675210
Disease: CONE-ROD DYSTROPHY 12 (disorder)
CONE-ROD DYSTROPHY 12 (disorder) 		1 0 1 3.2E-02 0 0
CUI: C2677516
Disease: RETINITIS PIGMENTOSA 41 (disorder)
RETINITIS PIGMENTOSA 41 (disorder) 		1 0 1 3.2E-02 0 0
CUI: C2936816
Disease: Micromelic dysplasia, congenital, with dislocation of radius
Micromelic dysplasia, congenital, with dislocation of radius 		1 0 1 3.2E-02 0 0
CUI: C0085569
Disease: Metabolic acidosis, NAG, acidifying salts
Metabolic acidosis, NAG, acidifying salts 		2 0 1 3.1E-02 0 0
CUI: C0349540
Disease: Astrocytoma of spinal cord
Astrocytoma of spinal cord 		2 0 1 3.1E-02 0 0