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: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 1.1E-02 0 0
3 beta-Hydroxysteroid dehydrogenase deficiency
9 0 1 6.7E-02 0 0
CUI: C4316788
Disease: Abnormality of the intestine
Abnormality of the intestine
19 0 1 4.0E-02 0 0
CUI: C0162309
Disease: Adrenoleukodystrophy
Adrenoleukodystrophy
294 0 1 3.3E-03 0 0
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
1377 0 1 7.2E-04 0 0
CUI: C0151849
Disease: Alkaline phosphatase raised
Alkaline phosphatase raised
55 0 1 1.6E-02 0 0
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
446 0 1 2.2E-03 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
3397 0 3 8.8E-04 0 0
CUI: C4551500
Disease: Amyloid Polyneuropathy, Iowa Type
Amyloid Polyneuropathy, Iowa Type
3 0 1 0.11 0 0
CUI: C4015843
Disease: AMYLOIDOSIS, CARDIAC AND CUTANEOUS
AMYLOIDOSIS, CARDIAC AND CUTANEOUS
2 0 1 0.12 0 0
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral
8 0 1 7.1E-02 0 0
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1
164 0 1 5.9E-03 0 0
CUI: C0002792
Disease: anaphylaxis
anaphylaxis
180 0 1 5.4E-03 0 0
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome
247 0 1 4.0E-03 0 0
CUI: C0002871
Disease: Anemia
Anemia
847 94 1 1.2E-03 1 1.0E-02
CUI: C2698117
Disease: Anisocyte Measurement
Anisocyte Measurement
15 0 1 4.8E-02 0 0
CUI: C0221278
Disease: Anisocytosis
Anisocytosis
16 0 1 4.5E-02 0 0
CUI: C0149955
Disease: Annular pancreas
Annular pancreas
19 0 1 4.0E-02 0 0
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
1410 0 1 7.1E-04 0 0
APOLIPOPROTEIN A-I (BALTIMORE) PHENOTYPE
2 0 1 0.12 0 0
APOLIPOPROTEIN A-I (MARBURG) PHENOTYPE
2 0 1 0.12 0 0
APOLIPOPROTEIN A-I (MUNSTER3B) PHENOTYPE
2 0 1 0.12 0 0
APOLIPOPROTEIN A-I (MUNSTER3C) PHENOTYPE
2 0 1 0.12 0 0
APOLIPOPROTEIN A-I (NORWAY) PHENOTYPE
2 0 1 0.12 0 0
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation
53 0 1 1.7E-02 0 0