Source: INFERRED ×
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: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 1.9E-02
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 1.9E-02
CUI: C1862591
Disease: CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO 		0 1 0 0 1 1.9E-02
CUI: C0025958
Disease: Microcephaly
Microcephaly 		855 0 1 1.1E-03 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		773 0 1 1.3E-03 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		734 0 1 1.3E-03 0 0
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		1458 0 2 1.3E-03 0 0
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		687 1622 1 1.4E-03 1 6.0E-04
CUI: C0038379
Disease: Strabismus
Strabismus 		682 0 1 1.4E-03 0 0
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		622 0 1 1.5E-03 0 0
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		1259 0 2 1.6E-03 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism 		574 0 1 1.7E-03 0 0
CUI: C0086543
Disease: Cataract
Cataract 		561 0 1 1.7E-03 0 0
CUI: C1384666
Disease: hearing impairment
hearing impairment 		551 0 1 1.7E-03 0 0
CUI: C0349588
Disease: Short stature
Short stature 		1122 0 2 1.7E-03 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia 		536 0 1 1.8E-03 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		508 0 1 1.9E-03 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism 		1039 0 2 1.9E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		491 0 1 1.9E-03 0 0
CUI: C0239234
Disease: Low set ears
Low set ears 		489 0 1 1.9E-03 0 0
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		1005 0 2 1.9E-03 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE 		476 0 1 2.0E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		470 0 1 2.0E-03 0 0
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		459 0 1 2.1E-03 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		942 0 2 2.1E-03 0 0