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: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans
64 0 1 1.3E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 3.1E-02 0 0
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction
90 0 1 9.8E-03 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia
43 0 1 1.8E-02 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria
76 0 1 1.1E-02 0 0
CUI: C0002448
Disease: Ameloblastoma
Ameloblastoma
174 0 1 5.4E-03 0 0
CUI: C0002622
Disease: Amnesia
Amnesia
173 0 1 5.4E-03 0 0
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
1114 0 1 8.9E-04 0 0
CUI: C0002793
Disease: Anaplasia
Anaplasia
538 0 1 1.8E-03 0 0
CUI: C0002874
Disease: Aplastic Anemia
Aplastic Anemia
238 0 1 4.0E-03 0 0
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
434 0 1 2.2E-03 0 0
CUI: C0002965
Disease: Angina, Unstable
Angina, Unstable
129 0 1 7.1E-03 0 0
CUI: C0003076
Disease: Aniridia
Aniridia
83 0 1 1.1E-02 0 0
CUI: C0003119
Disease: Anophthalmos
Anophthalmos
89 0 1 9.9E-03 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
139 0 1 6.6E-03 0 0
CUI: C0003504
Disease: Aortic Valve Insufficiency
Aortic Valve Insufficiency
377 0 1 2.6E-03 0 0
CUI: C0003537
Disease: Aphasia
Aphasia
86 0 1 1.0E-02 0 0
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation
53 0 1 1.5E-02 0 0
CUI: C0003851
Disease: Arteriosclerosis Obliterans
Arteriosclerosis Obliterans
49 0 1 1.6E-02 0 0
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic
450 0 1 2.2E-03 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
198 0 1 4.8E-03 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism
148 0 1 6.3E-03 0 0
CUI: C0004144
Disease: Atelectasis
Atelectasis
62 0 1 1.4E-02 0 0
CUI: C0004368
Disease: Autoimmune state
Autoimmune state
70 0 1 1.2E-02 0 0