Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Ventricular Outflow Obstruction, Left
0 1 0 0 1 2.8E-03
Erythrocytosis due to low atmospheric pressure
0 13 0 0 2 5.5E-03
Delayed speech and language development
560 0 1 1.6E-03 0 0
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy
454 0 1 1.9E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
433 0 1 1.9E-03 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
362 0 1 2.3E-03 0 0
CUI: C0851578
Disease: Sleep Disorders
Sleep Disorders
360 0 1 2.3E-03 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression
333 0 1 2.4E-03 0 0
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures
300 0 1 2.6E-03 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
291 0 1 2.7E-03 0 0
CUI: C1865014
Disease: Long philtrum
Long philtrum
282 0 1 2.7E-03 0 0
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
272 0 1 2.8E-03 0 0
CUI: C0022578
Disease: Keratoconus
Keratoconus
269 0 1 2.8E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche
267 0 1 2.9E-03 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus
265 0 1 2.9E-03 0 0
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
610 0 2 2.9E-03 0 0
Clear-cell metastatic renal cell carcinoma
260 0 1 2.9E-03 0 0
CUI: C0008350
Disease: Cholelithiasis
Cholelithiasis
252 0 1 3.0E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 3.0E-03 0 0
CUI: C0333307
Disease: Superficial ulcer
Superficial ulcer
242 0 1 3.1E-03 0 0
CUI: C0700201
Disease: Dyssomnias
Dyssomnias
236 0 1 3.1E-03 0 0
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss
235 0 1 3.2E-03 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia
226 0 1 3.2E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
219 0 1 3.3E-03 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia
218 0 1 3.3E-03 0 0