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 2.3E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 2.4E-03
CUI: C0036904
Disease: Sexual desire disorder
Sexual desire disorder
0 1 0 0 1 2.4E-03
CUI: C0234512
Disease: Prosopagnosia
Prosopagnosia
0 2 0 0 2 4.8E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 2.4E-03
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 2.3E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder)
0 1 0 0 1 2.4E-03
CUI: C1869116
Disease: ASTHMA, SUSCEPTIBILITY TO (finding)
ASTHMA, SUSCEPTIBILITY TO (finding)
0 3 0 0 1 2.4E-03
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft
0 2 0 0 2 4.8E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 2.4E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 2.4E-03
Frequent episodic tension-type headache
0 1 0 0 1 2.4E-03
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 2.3E-03
CUI: C0231835
Disease: Tachypnea
Tachypnea
82 0 1 1.1E-03 0 0
CUI: C1314665
Disease: Serum alkaline phosphatase raised
Serum alkaline phosphatase raised
67 0 1 1.1E-03 0 0
Familial Nonmedullary Thyroid Cancer
66 0 1 1.1E-03 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
59 0 1 1.1E-03 0 0
CUI: C0151849
Disease: Alkaline phosphatase raised
Alkaline phosphatase raised
55 0 1 1.1E-03 0 0
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
55 0 1 1.1E-03 0 0
CUI: C1275278
Disease: Extraskeletal Myxoid Chondrosarcoma
Extraskeletal Myxoid Chondrosarcoma
50 0 1 1.1E-03 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance
44 0 1 1.1E-03 0 0
CUI: C0266399
Disease: Infantile uterus
Infantile uterus
43 0 1 1.1E-03 0 0
CUI: C0007965
Disease: Chediak-Higashi Syndrome
Chediak-Higashi Syndrome
41 0 1 1.1E-03 0 0
CUI: C0008525
Disease: Choroideremia
Choroideremia
41 0 1 1.1E-03 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia
41 0 1 1.1E-03 0 0