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 1.4E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence
645 0 1 1.4E-03 0 0
Red cell distribution width determination
593 0 1 1.5E-03 0 0
RDW - Red blood cell distribution width result
593 0 1 1.5E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 1 1.6E-03 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 1 1.7E-03 0 0
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness
536 0 1 1.7E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 1.8E-03 0 0
CUI: C0013421
Disease: Dystonia
Dystonia
453 0 1 2.0E-03 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
955 0 2 2.0E-03 0 0
CUI: C0023530
Disease: Leukopenia
Leukopenia
440 0 1 2.0E-03 0 0
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
439 0 1 2.0E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 4 2.0E-03 0 0
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus
417 0 1 2.1E-03 0 0
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay
393 0 1 2.2E-03 0 0
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
843 0 2 2.2E-03 0 0
CUI: C1854301
Disease: Motor delay
Motor delay
384 0 1 2.3E-03 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression
333 0 1 2.6E-03 0 0
CUI: C0242596
Disease: Neoplasm, Residual
Neoplasm, Residual
329 0 1 2.6E-03 0 0
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder
328 0 1 2.6E-03 0 0
CUI: C0014038
Disease: Encephalitis
Encephalitis
324 0 1 2.6E-03 0 0
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia
320 0 1 2.7E-03 0 0
CUI: C0007682
Disease: CNS disorder
CNS disorder
319 0 1 2.7E-03 0 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity
319 0 1 2.7E-03 0 0
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency
315 0 1 2.7E-03 0 0