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: C0232310
Disease: P mitrale (finding)
P mitrale (finding)
3 0 1 0.33 0 0
CUI: C0238705
Disease: Left atrial hypertrophy
Left atrial hypertrophy
3 0 1 0.33 0 0
CUI: C0520888
Disease: Inverted T wave
Inverted T wave
4 0 1 0.25 0 0
CUI: C0344955
Disease: Ventricular septal hypertrophy
Ventricular septal hypertrophy
8 3 1 0.12 1 1.0E-01
CARDIOMYOPATHY, INFANTILE HYPERTROPHIC
9 0 1 0.11 0 0
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
9 163 1 0.11 1 5.9E-03
CUI: C0553980
Disease: Endomyocardial Fibrosis
Endomyocardial Fibrosis
20 0 1 5.0E-02 0 0
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
21 0 1 4.8E-02 0 0
CUI: C0266258
Disease: Congenital absence of liver
Congenital absence of liver
25 0 1 4.0E-02 0 0
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria
30 0 1 3.3E-02 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy
41 0 1 2.4E-02 0 0
CUI: C0751951
Disease: Central Core Myopathy (disorder)
Central Core Myopathy (disorder)
44 0 1 2.3E-02 0 0
CUI: C0008928
Disease: Cleidocranial Dysplasia
Cleidocranial Dysplasia
52 0 1 1.9E-02 0 0
CUI: C3160712
Disease: Palpitations, CTCAE
Palpitations, CTCAE
64 0 1 1.6E-02 0 0
CUI: C0030252
Disease: Palpitations
Palpitations
70 0 1 1.4E-02 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria
76 0 1 1.3E-02 0 0
Cardiomyopathy, Hypertrophic, Familial
83 355 1 1.2E-02 3 8.3E-03
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation
96 0 1 1.0E-02 0 0
CUI: C0231807
Disease: Dyspnea on exertion
Dyspnea on exertion
102 0 1 9.8E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
131 0 1 7.6E-03 0 0
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death
133 0 1 7.5E-03 0 0
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
146 0 1 6.8E-03 0 0
Hypertrophic obstructive cardiomyopathy
233 0 1 4.3E-03 0 0
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis
254 0 1 3.9E-03 0 0
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
267 0 1 3.7E-03 0 0