Source: ALL
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: C0019295
Disease: Inguinal Hernia, Direct
Inguinal Hernia, Direct 		1 0 1 3.8E-02 0 0
CUI: C0262665
Disease: Abnormal vocal cord morphology
Abnormal vocal cord morphology 		1 2 1 3.8E-02 2 0.22
CUI: C0265669
Disease: Congenital dislocation of knee
Congenital dislocation of knee 		1 0 1 3.8E-02 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis 		1 0 1 3.8E-02 0 0
CUI: C0333454
Disease: Granulovacuolar degeneration
Granulovacuolar degeneration 		1 0 1 3.8E-02 0 0
CUI: C0341266
Disease: Diverticulosis of the duodenum
Diverticulosis of the duodenum 		1 1 1 3.8E-02 1 0.11
CUI: C0432201
Disease: Boomerang dysplasia
Boomerang dysplasia 		1 0 1 3.8E-02 0 0
CUI: C0478074
Disease: Other congenital malformations of spine, not associated with scoliosis
Other congenital malformations of spine, not associated with scoliosis 		1 0 1 3.8E-02 0 0
CUI: C0751421
Disease: Hemispatial Neglect
Hemispatial Neglect 		1 0 1 3.8E-02 0 0
CUI: C0860515
Disease: Freezing of gait
Freezing of gait 		1 0 1 3.8E-02 0 0
CUI: C0878565
Disease: Electrocardiogram J wave
Electrocardiogram J wave 		1 0 1 3.8E-02 0 0
CUI: C1321325
Disease: Elliptical nystagmus
Elliptical nystagmus 		1 0 1 3.8E-02 0 0
CUI: C1834559
Disease: Continuous Muscle Fiber Activity, Hereditary
Continuous Muscle Fiber Activity, Hereditary 		1 0 1 3.8E-02 0 0
CUI: C1836151
Disease: Frontolimbic dementia
Frontolimbic dementia 		1 0 1 3.8E-02 0 0
CUI: C1836447
Disease: Nemaline myopathy 4
Nemaline myopathy 4 		1 0 1 3.8E-02 0 0
CUI: C1838313
Disease: Pick Complex
Pick Complex 		1 0 1 3.8E-02 0 0
CUI: C1839909
Disease: CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED
CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED 		1 0 1 3.8E-02 0 0
CUI: C1844006
Disease: Hydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction
Hydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction 		1 0 1 3.8E-02 0 0
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		1 0 1 3.8E-02 0 0
CUI: C1853188
Disease: Interhemispheric cysts
Interhemispheric cysts 		1 0 1 3.8E-02 0 0
CUI: C1853736
Disease: Congenital Disorder Of Glycosylation, Type IIB
Congenital Disorder Of Glycosylation, Type IIB 		1 0 1 3.8E-02 0 0
CUI: C1853755
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY
INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY 		1 0 1 3.8E-02 0 0
CUI: C1860896
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6 		1 0 1 3.8E-02 0 0
CUI: C1862415
Disease: Cervical segmentation defect
Cervical segmentation defect 		1 0 1 3.8E-02 0 0
CUI: C1862420
Disease: Tombstone-shaped proximal phalanges
Tombstone-shaped proximal phalanges 		1 0 1 3.8E-02 0 0