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: C4310739
Disease: OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME 		1 0 1 0.20 0 0
CUI: C0152077
Disease: Dyshormonogenic goiter
Dyshormonogenic goiter 		3 0 1 0.14 0 0
CUI: C2697999
Disease: Macrophage Colony Stimulating Factor Measurement
Macrophage Colony Stimulating Factor Measurement 		3 0 1 0.14 0 0
CUI: C4329989
Disease: Feline Oral Squamous Cell Carcinoma
Feline Oral Squamous Cell Carcinoma 		3 0 1 0.14 0 0
CUI: C1321809
Disease: HYPOTHYROIDISM, GOITROUS
HYPOTHYROIDISM, GOITROUS 		5 0 1 0.11 0 0
CUI: C1971021
Disease: Potassium depletion
Potassium depletion 		6 0 1 1.0E-01 0 0
CUI: C3827253
Disease: Classical Glioblastoma
Classical Glioblastoma 		6 0 1 1.0E-01 0 0
CUI: C0523829
Disease: Phosphatidylcholine measurement
Phosphatidylcholine measurement 		9 0 1 7.7E-02 0 0
CUI: C0342191
Disease: Familial dyshormonogenetic goiter
Familial dyshormonogenetic goiter 		11 0 1 6.7E-02 0 0
CUI: C3893645
Disease: response to ACE inhibitor
response to ACE inhibitor 		15 0 1 5.3E-02 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 2 4.7E-02 0 0
CUI: C1704380
Disease: Distal Renal Tubular Acidosis
Distal Renal Tubular Acidosis 		23 0 1 3.7E-02 0 0
CUI: C0025309
Disease: Meningoencephalitis
Meningoencephalitis 		30 0 1 2.9E-02 0 0
CUI: C0340164
Disease: Lofgrens syndrome
Lofgrens syndrome 		30 0 1 2.9E-02 0 0
CUI: C0391957
Disease: idiopathic epilepsy
idiopathic epilepsy 		30 0 1 2.9E-02 0 0
CUI: C1854310
Disease: Hypotrichosis simplex
Hypotrichosis simplex 		37 0 1 2.4E-02 0 0
CUI: C2749675
Disease: Cortical gyral simplification
Cortical gyral simplification 		39 0 1 2.3E-02 0 0
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma 		41 0 1 2.2E-02 0 0
CUI: C0242387
Disease: Mandibulofacial Dysostosis
Mandibulofacial Dysostosis 		42 0 1 2.2E-02 0 0
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		90 0 2 2.2E-02 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 1 2.0E-02 0 0
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 0 1 1.8E-02 0 0
CUI: C0220726
Disease: Diastrophic dysplasia
Diastrophic dysplasia 		56 0 1 1.7E-02 0 0
CUI: C0020621
Disease: Hypokalemia
Hypokalemia 		61 0 1 1.5E-02 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 1 1.4E-02 0 0