Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Finding of Mean Corpuscular Hemoglobin
653 0 1 1.3E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
433 0 1 1.8E-03 0 0
CUI: C0282160
Disease: Aplasia Cutis Congenita
Aplasia Cutis Congenita
393 0 1 2.0E-03 0 0
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
338 0 1 2.2E-03 0 0
CUI: C0153633
Disease: Malignant neoplasm of brain
Malignant neoplasm of brain
294 0 1 2.4E-03 0 0
CUI: C1960398
Disease: HER2-positive carcinoma of breast
HER2-positive carcinoma of breast
288 0 1 2.5E-03 0 0
CUI: C0007095
Disease: Carcinoid Tumor
Carcinoid Tumor
267 0 1 2.6E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior
261 0 1 2.6E-03 0 0
CUI: C0489786
Disease: Height
Height
249 0 1 2.7E-03 0 0
CUI: C3642347
Disease: Basal-Like Breast Carcinoma
Basal-Like Breast Carcinoma
245 0 1 2.8E-03 0 0
Leukoencephalopathy, Progressive Multifocal
240 0 1 2.8E-03 0 0
CUI: C2004493
Disease: Leukemia, B-Cell
Leukemia, B-Cell
239 0 1 2.8E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 2.8E-03 0 0
Red cell distribution width determination
593 0 2 2.8E-03 0 0
RDW - Red blood cell distribution width result
593 0 2 2.8E-03 0 0
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss
235 0 1 2.8E-03 0 0
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
234 0 1 2.8E-03 0 0
CUI: C0268398
Disease: Familial lichen amyloidosis
Familial lichen amyloidosis
230 0 1 2.9E-03 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal
227 0 1 2.9E-03 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia
226 0 1 2.9E-03 0 0
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
565 0 2 2.9E-03 0 0
CUI: C0858252
Disease: Breast adenocarcinoma
Breast adenocarcinoma
219 0 1 3.0E-03 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis
217 0 1 3.0E-03 0 0
CUI: C0033999
Disease: Pterygium
Pterygium
216 0 1 3.0E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 3.0E-03 0 0