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: C0029134
Disease: Optic Neuritis
Optic Neuritis
0 4 0 0 1 5.0E-02
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern
0 743 0 0 1 1.3E-03
Red cell distribution width determination
593 0 1 1.6E-03 0 0
RDW - Red blood cell distribution width result
593 0 1 1.6E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
580 0 1 1.6E-03 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
429 0 1 2.1E-03 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
426 0 1 2.1E-03 0 0
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly
410 0 1 2.2E-03 0 0
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease
365 0 1 2.4E-03 0 0
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
338 0 1 2.6E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus
716 0 2 2.6E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 0 1 2.7E-03 0 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity
319 0 1 2.7E-03 0 0
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome
316 0 1 2.8E-03 0 0
CUI: C0042963
Disease: Vomiting
Vomiting
303 0 1 2.9E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence
645 0 2 2.9E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
272 0 1 3.2E-03 0 0
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy
271 0 1 3.2E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability
854 0 3 3.3E-03 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
251 0 1 3.4E-03 0 0
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
249 0 1 3.4E-03 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 2 3.4E-03 0 0
Differentiated Thyroid Gland Carcinoma
245 0 1 3.4E-03 0 0
CUI: C0022346
Disease: Icterus
Icterus
241 0 1 3.5E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 3.5E-03 0 0