Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 2.9E-02
CORONARY ARTERY DISEASE, MODIFIER OF
0 1 0 0 1 2.9E-02
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
0 1 0 0 1 2.9E-02
CUI: C3825385
Disease: Epilepsy in adolescence
Epilepsy in adolescence
0 1 0 0 1 2.9E-02
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO
0 1 0 0 1 2.9E-02
Corpuscular Hemoglobin Concentration Mean
401 0 1 1.7E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
272 1169 1 2.2E-03 1 8.3E-04
CUI: C0005612
Disease: Birth Weight
Birth Weight
214 0 1 2.5E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
166 0 1 2.9E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
166 0 1 2.9E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
166 0 1 2.9E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
165 0 1 2.9E-03 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism
148 0 1 3.0E-03 0 0
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
145 0 1 3.0E-03 0 0
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow
141 0 1 3.1E-03 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition
140 0 1 3.1E-03 0 0
Platelet Component Distribution Width Measurement
134 0 1 3.2E-03 0 0
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
131 0 1 3.2E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
131 0 1 3.2E-03 0 0
CUI: C0085078
Disease: Lysosomal Storage Diseases
Lysosomal Storage Diseases
130 0 1 3.2E-03 0 0
CUI: C0266544
Disease: Microcornea
Microcornea
129 0 1 3.2E-03 0 0
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly
123 0 1 3.3E-03 0 0
CUI: C3805574
Disease: Increased fracture rate
Increased fracture rate
123 0 1 3.3E-03 0 0
CUI: C3714581
Disease: Multicystic Dysplastic Kidney
Multicystic Dysplastic Kidney
121 0 1 3.3E-03 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly
120 0 1 3.3E-03 0 0