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: C0741146
Disease: anxiety acute
anxiety acute 		1 0 1 1.0E-01 0 0
CUI: C1834478
Disease: MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS
MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS 		1 0 1 1.0E-01 0 0
CUI: C1842035
Disease: Giant Platelet Syndrome with Thrombocytopenia
Giant Platelet Syndrome with Thrombocytopenia 		1 0 1 1.0E-01 0 0
CUI: C1844516
Disease: Increased density of long bone diaphyses
Increased density of long bone diaphyses 		1 0 1 1.0E-01 0 0
CUI: C1844519
Disease: Partial fusion of carpals
Partial fusion of carpals 		1 0 1 1.0E-01 0 0
CUI: C1844520
Disease: Partial fusion of tarsals
Partial fusion of tarsals 		1 0 1 1.0E-01 0 0
CUI: C1844702
Disease: Vertical clivus
Vertical clivus 		1 0 1 1.0E-01 0 0
CUI: C1844712
Disease: Nonossified fifth metatarsal
Nonossified fifth metatarsal 		1 0 1 1.0E-01 0 0
CUI: C1845235
Disease: Heterotopia, Periventricular, Ehlers-Danlos Variant
Heterotopia, Periventricular, Ehlers-Danlos Variant 		1 0 1 1.0E-01 0 0
CUI: C1846129
Disease: Terminal Osseous Dysplasia and Pigmentary Defects
Terminal Osseous Dysplasia and Pigmentary Defects 		1 0 1 1.0E-01 0 0
CUI: C1847711
Disease: NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO
NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO 		1 0 1 1.0E-01 0 0
CUI: C1861512
Disease: Cochleosaccular degeneration of the inner ear and progressive cataracts
Cochleosaccular degeneration of the inner ear and progressive cataracts 		1 0 1 1.0E-01 0 0
CUI: C1862136
Disease: Abnormality of the tarsal bones
Abnormality of the tarsal bones 		1 0 1 1.0E-01 0 0
CUI: C1863659
Disease: DEAFNESS, AUTOSOMAL DOMINANT 17
DEAFNESS, AUTOSOMAL DOMINANT 17 		1 0 1 1.0E-01 0 0
CUI: C1866737
Disease: Lateral femoral bowing
Lateral femoral bowing 		1 0 1 1.0E-01 0 0
CUI: C2239253
Disease: Sinus of Valsalva aneurysm
Sinus of Valsalva aneurysm 		1 0 1 1.0E-01 0 0
CUI: C2746068
Disease: Congenital idiopathic intestinal pseudoobstruction
Congenital idiopathic intestinal pseudoobstruction 		1 0 1 1.0E-01 0 0
CUI: C2748918
Disease: Otopalatodigital Spectrum Disorder
Otopalatodigital Spectrum Disorder 		1 0 1 1.0E-01 0 0
CUI: C2931716
Disease: Deafness, autosomal dominant nonsyndromic sensorineural 17
Deafness, autosomal dominant nonsyndromic sensorineural 17 		1 0 1 1.0E-01 0 0
CUI: C3160906
Disease: Subependymal nodular heterotopia
Subependymal nodular heterotopia 		1 0 1 1.0E-01 0 0
CUI: C3554663
Disease: BLEEDING DISORDER, PLATELET-TYPE, 15
BLEEDING DISORDER, PLATELET-TYPE, 15 		1 0 1 1.0E-01 0 0
CUI: C3854603
Disease: FNAITP
FNAITP 		12 0 2 1.0E-01 0 0
CUI: C4021189
Disease: Underdeveloped superior crus of antihelix
Underdeveloped superior crus of antihelix 		1 0 1 1.0E-01 0 0
CUI: C4021253
Disease: Undulate clavicles
Undulate clavicles 		1 0 1 1.0E-01 0 0
CUI: C4021547
Disease: Neutrophil inclusion bodies
Neutrophil inclusion bodies 		1 0 1 1.0E-01 0 0