Source: CLINVAR ×
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: C1837317
Disease: Alpha-B Crystallinopathy
Alpha-B Crystallinopathy 		1 0 1 0.50 0 0
CUI: C1860752
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 		1 12 1 0.50 5 0.29
CUI: C2678474
Disease: CARDIOMYOPATHY, DILATED, 2A (disorder)
CARDIOMYOPATHY, DILATED, 2A (disorder) 		1 2 1 0.50 2 0.20
CUI: C2750091
Disease: Cardiomyopathy, Dilated, 1FF
Cardiomyopathy, Dilated, 1FF 		1 5 1 0.50 3 0.25
CUI: C3151236
Disease: MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED
MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED 		1 0 1 0.50 0 0
CUI: C3554649
Disease: CARDIOMYOPATHY, DILATED, 1II
CARDIOMYOPATHY, DILATED, 1II 		1 3 1 0.50 1 8.3E-02
CUI: C3808377
Disease: CATARACT 16, MULTIPLE TYPES
CATARACT 16, MULTIPLE TYPES 		1 0 1 0.50 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		6 15 1 0.14 2 8.7E-02
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		7 0 1 0.12 0 0
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		45 172 2 4.4E-02 1 5.5E-03
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		24 332 1 4.0E-02 5 1.5E-02
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		29 468 1 3.3E-02 6 1.3E-02
CUI: C0009691
Disease: Congenital cataract
Congenital cataract 		32 0 1 3.0E-02 0 0
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		43 0 1 2.3E-02 0 0