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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.6E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.9E-02
CUI: C0234512
Disease: Prosopagnosia
Prosopagnosia 		0 2 0 0 1 1.8E-02
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 1.8E-02
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon 		0 1 0 0 1 1.9E-02
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 1.9E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.9E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.9E-02
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 1.9E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 1.6E-02
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		295 0 1 2.3E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 2.7E-03 0 0
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		228 0 1 2.7E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 1 2.8E-03 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia 		218 0 1 2.8E-03 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		217 0 1 2.8E-03 0 0
CUI: C0023269
Disease: leiomyosarcoma
leiomyosarcoma 		213 0 1 2.8E-03 0 0
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase 		212 0 1 2.8E-03 0 0
CUI: C2981150
Disease: Uranostaphyloschisis
Uranostaphyloschisis 		190 75 1 3.0E-03 1 7.8E-03
CUI: C0205699
Disease: Carcinomatosis
Carcinomatosis 		186 0 1 3.1E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 3.1E-03 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		171 0 1 3.2E-03 0 0
CUI: C1512981
Disease: Mammary Tumorigenesis
Mammary Tumorigenesis 		162 0 1 3.3E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 3.3E-03 0 0
CUI: C0206667
Disease: Adrenal Cortical Adenoma
Adrenal Cortical Adenoma 		156 0 1 3.4E-03 0 0