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: C0035934
Disease: Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome 		31 0 9 0.12 0 0
CUI: C0008928
Disease: Cleidocranial Dysplasia
Cleidocranial Dysplasia 		52 0 9 9.5E-02 0 0
CUI: C3887980
Disease: Protanomaly
Protanomaly 		19 0 6 9.2E-02 0 0
CUI: C2674219
Disease: SPHEROCYTOSIS, HEREDITARY, 2
SPHEROCYTOSIS, HEREDITARY, 2 		8 0 5 9.1E-02 0 0
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		29 0 6 8.0E-02 0 0
CUI: C2825306
Disease: Treatment related leukaemia
Treatment related leukaemia 		30 0 6 7.9E-02 0 0
CUI: C0036211
Disease: Sarcoma 180
Sarcoma 180 		20 0 5 7.5E-02 0 0
CUI: C0032339
Disease: Rothmund-Thomson syndrome
Rothmund-Thomson syndrome 		35 0 6 7.4E-02 0 0
CUI: C3831784
Disease: Acute monocytic/monoblastic leukemia
Acute monocytic/monoblastic leukemia 		35 0 6 7.4E-02 0 0
CUI: C0457334
Disease: Acute monoblastic leukemia
Acute monoblastic leukemia 		37 0 6 7.2E-02 0 0
CUI: C0598894
Disease: Monocytic leukemia
Monocytic leukemia 		71 0 8 7.0E-02 0 0
CUI: C4076240
Disease: Chronic kidney disease mineral and bone disorder
Chronic kidney disease mineral and bone disorder 		26 0 5 6.8E-02 0 0
CUI: C1292780
Disease: Therapy-related myelodysplastic syndrome
Therapy-related myelodysplastic syndrome 		42 0 6 6.8E-02 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome 		15 0 4 6.3E-02 0 0
CUI: C0242225
Disease: Color blindness
Color blindness 		33 0 5 6.2E-02 0 0
CUI: C0023479
Disease: Acute myelomonocytic leukemia
Acute myelomonocytic leukemia 		105 0 9 6.1E-02 0 0
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		73 0 7 5.9E-02 0 0
CUI: C3149841
Disease: POLYCYSTIC KIDNEY DISEASE 1
POLYCYSTIC KIDNEY DISEASE 1 		39 0 5 5.8E-02 0 0
CUI: C0302486
Disease: Erythrophagocytosis
Erythrophagocytosis 		40 0 5 5.7E-02 0 0
CUI: C4688007
Disease: Platinum-Resistant Ovarian Carcinoma
Platinum-Resistant Ovarian Carcinoma 		41 0 5 5.7E-02 0 0
CUI: C0585216
Disease: Alpha-Thalassemia Myelodysplasia Syndrome
Alpha-Thalassemia Myelodysplasia Syndrome 		4 0 3 5.7E-02 0 0
CUI: C1860707
Disease: TUBEROUS SCLEROSIS 2 (disorder)
TUBEROUS SCLEROSIS 2 (disorder) 		43 0 5 5.6E-02 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation 		505 0 29 5.5E-02 0 0
CUI: C1336735
Disease: Treatment related acute myeloid leukaemia
Treatment related acute myeloid leukaemia 		65 0 6 5.4E-02 0 0
CUI: C3161174
Disease: Hemoglobin H Disease
Hemoglobin H Disease 		29 0 4 5.2E-02 0 0