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: C0035281
Disease: Retention cyst
Retention cyst 		1 0 1 7.7E-02 0 0
CUI: C0232874
Disease: Febrile proteinuria
Febrile proteinuria 		1 0 1 7.7E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 7.7E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 7.7E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 7.7E-02 0 0
CUI: C0268916
Disease: Atrophy of vas deferens
Atrophy of vas deferens 		1 0 1 7.7E-02 0 0
CUI: C0342483
Disease: Hyperreninemic hypoaldosteronism
Hyperreninemic hypoaldosteronism 		1 0 1 7.7E-02 0 0
CUI: C0400875
Disease: Hollow visceral neuropathy
Hollow visceral neuropathy 		1 0 1 7.7E-02 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 7.7E-02 0 0
CUI: C0852085
Disease: Congenital connective tissue disorder
Congenital connective tissue disorder 		1 0 1 7.7E-02 0 0
CUI: C0935909
Disease: Breast Carcinoma Metastatic in the Skin
Breast Carcinoma Metastatic in the Skin 		1 0 1 7.7E-02 0 0
CUI: C1112654
Disease: Peripheral artery dissection
Peripheral artery dissection 		1 0 1 7.7E-02 0 0
CUI: C1270206
Disease: Desmoplastic mesothelioma
Desmoplastic mesothelioma 		1 0 1 7.7E-02 0 0
CUI: C1622439
Disease: Lentiglobus
Lentiglobus 		1 0 1 7.7E-02 0 0
CUI: C1832168
Disease: BLOOD GROUP--FROESE
BLOOD GROUP--FROESE 		1 0 1 7.7E-02 0 0
CUI: C1835130
Disease: Premature calcification of mitral annulus
Premature calcification of mitral annulus 		1 0 1 7.7E-02 0 0
CUI: C1858626
Disease: Bicarbonate-wasting renal tubular acidosis
Bicarbonate-wasting renal tubular acidosis 		1 0 1 7.7E-02 0 0
CUI: C1858628
Disease: Increased red cell osmotic resistance
Increased red cell osmotic resistance 		1 0 1 7.7E-02 0 0
CUI: C1861456
Disease: Stiff Skin Syndrome
Stiff Skin Syndrome 		1 0 1 7.7E-02 0 0
CUI: C1862190
Disease: BLOOD GROUP--WRIGHT ANTIGEN
BLOOD GROUP--WRIGHT ANTIGEN 		1 0 1 7.7E-02 0 0
CUI: C1862191
Disease: BLOOD GROUP--WALDNER TYPE
BLOOD GROUP--WALDNER TYPE 		1 0 1 7.7E-02 0 0
CUI: C1969039
Disease: Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology
Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology 		1 0 1 7.7E-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 5 1 7.7E-02 3 0.50
CUI: C2675212
Disease: Spherocytosis, Type 4
Spherocytosis, Type 4 		1 0 1 7.7E-02 0 0
CUI: C2713392
Disease: Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency
Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency 		1 0 1 7.7E-02 0 0