Source: CURATED ×
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: C0398777
Disease: Complement Factor H Deficiency
Complement Factor H Deficiency 		1 0 1 4.3E-02 0 0
CUI: C0497406
Disease: Overweight
Overweight 		1 0 1 4.3E-02 0 0
CUI: C0730295
Disease: BASAL LAMINAR DRUSEN (disorder)
BASAL LAMINAR DRUSEN (disorder) 		1 0 1 4.3E-02 0 0
CUI: C0751437
Disease: Adenohypophyseal Diseases
Adenohypophyseal Diseases 		1 0 1 4.3E-02 0 0
CUI: C0751438
Disease: Posterior pituitary disease
Posterior pituitary disease 		1 0 1 4.3E-02 0 0
CUI: C1332655
Disease: Complement component 3 deficiency
Complement component 3 deficiency 		1 0 1 4.3E-02 0 0
CUI: C1390474
Disease: Increased susceptibility to fractures
Increased susceptibility to fractures 		1 0 1 4.3E-02 0 0
CUI: C1832916
Disease: Timothy syndrome
Timothy syndrome 		1 0 1 4.3E-02 0 0
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		1 0 1 4.3E-02 0 0
CUI: C1842090
Disease: Platelet Glycoprotein IV Deficiency
Platelet Glycoprotein IV Deficiency 		1 0 1 4.3E-02 0 0
CUI: C1843542
Disease: T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC
T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC 		1 0 1 4.3E-02 0 0
CUI: C1853147
Disease: MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)
MACULAR DEGENERATION, AGE-RELATED, 4 (disorder) 		1 0 1 4.3E-02 0 0
CUI: C1855772
Disease: Absent corpus callosum cataract immunodeficiency
Absent corpus callosum cataract immunodeficiency 		1 0 1 4.3E-02 0 0
CUI: C1858085
Disease: Malar flattening
Malar flattening 		1 0 1 4.3E-02 0 0
CUI: C1861284
Disease: Immunodeficiency due to Defect in CD3-Epsilon
Immunodeficiency due to Defect in CD3-Epsilon 		1 0 1 4.3E-02 0 0
CUI: C1876175
Disease: Ataxia-Telangiectasia Variant
Ataxia-Telangiectasia Variant 		1 0 1 4.3E-02 0 0
CUI: C1969651
Disease: Macular Degeneration, Age-Related, 9
Macular Degeneration, Age-Related, 9 		1 0 1 4.3E-02 0 0
CUI: C2678478
Disease: Brugada Syndrome 3
Brugada Syndrome 3 		1 0 1 4.3E-02 0 0
CUI: C2752037
Disease: HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5 		1 0 1 4.3E-02 0 0
CUI: C2931299
Disease: ZAP70 deficiency
ZAP70 deficiency 		1 0 1 4.3E-02 0 0
CUI: C2931320
Disease: T cell immunodeficiency primary
T cell immunodeficiency primary 		1 0 1 4.3E-02 0 0
CUI: C3151071
Disease: COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE
COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE 		1 0 1 4.3E-02 0 0
CUI: C3151080
Disease: COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II 		1 0 1 4.3E-02 0 0
CUI: C3151081
Disease: COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I 		1 0 1 4.3E-02 0 0
CUI: C3151189
Disease: C9 Deficiency
C9 Deficiency 		1 0 1 4.3E-02 0 0