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: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		3 0 2 0.14 0 0
CUI: C1863052
Disease: ALZHEIMER DISEASE, FAMILIAL, 1
ALZHEIMER DISEASE, FAMILIAL, 1 		4 0 2 0.13 0 0
CUI: C0751249
Disease: Chronic Insomnia
Chronic Insomnia 		6 0 2 0.12 0 0
CUI: C4721845
Disease: Marfan Syndrome, Type I
Marfan Syndrome, Type I 		11 0 2 9.1E-02 0 0
CUI: C0205858
Disease: General Paralysis
General Paralysis 		12 0 2 8.7E-02 0 0
CUI: C0393911
Disease: Pure Autonomic Failure
Pure Autonomic Failure 		12 0 2 8.7E-02 0 0
CUI: C0268314
Disease: Cholestasis-edema syndrome, Norwegian type
Cholestasis-edema syndrome, Norwegian type 		14 0 2 8.0E-02 0 0
CUI: C0018944
Disease: Hematoma
Hematoma 		1 0 1 7.7E-02 0 0
CUI: C0278776
Disease: recurrent childhood acute myeloid leukemia
recurrent childhood acute myeloid leukemia 		1 0 1 7.7E-02 0 0
CUI: C0342610
Disease: Hereditary cerebrovascular amyloidosis
Hereditary cerebrovascular amyloidosis 		1 0 1 7.7E-02 0 0
CUI: C0558193
Disease: Stiff limbs
Stiff limbs 		1 0 1 7.7E-02 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system 		1 0 1 7.7E-02 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis 		1 0 1 7.7E-02 0 0
CUI: C1297882
Disease: Partial Trisomy
Partial Trisomy 		29 0 3 7.7E-02 0 0
CUI: C1321782
Disease: Gestosis
Gestosis 		1 0 1 7.7E-02 0 0
CUI: C1334068
Disease: Hypercellular bone marrow
Hypercellular bone marrow 		1 0 1 7.7E-02 0 0
CUI: C1968537
Disease: Severe speech delay
Severe speech delay 		1 0 1 7.7E-02 0 0
CUI: C2677087
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5 		1 0 1 7.7E-02 0 0
CUI: C2751494
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT 		1 0 1 7.7E-02 0 0
CUI: C2751536
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED 		1 0 1 7.7E-02 0 0
CUI: C3150967
Disease: KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT
KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT 		1 0 1 7.7E-02 0 0
CUI: C3150969
Disease: MICROPHTHALMIA, ISOLATED 7
MICROPHTHALMIA, ISOLATED 7 		1 0 1 7.7E-02 0 0
CUI: C3276611
Disease: Absent or delayed speech development
Absent or delayed speech development 		1 0 1 7.7E-02 0 0
CUI: C3279839
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 7
MENTAL RETARDATION, AUTOSOMAL DOMINANT 7 		1 0 1 7.7E-02 0 0
CUI: C3888307
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT 		1 0 1 7.7E-02 0 0