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: C1838329
Disease: APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS
APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS 		0 5 0 0 1 2.2E-02
CUI: C2674723
Disease: RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER 		0 14 0 0 1 1.8E-02
CUI: C3809609
Disease: PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES
PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES 		0 2 0 0 1 2.3E-02
CUI: C0005938
Disease: Bone Density
Bone Density 		138 0 1 1.8E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 1.9E-03 0 0
CUI: C0033774
Disease: Pruritus
Pruritus 		107 0 1 1.9E-03 0 0
CUI: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear 		95 0 1 1.9E-03 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls 		94 0 1 1.9E-03 0 0
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		93 0 1 2.0E-03 0 0
CUI: C0349506
Disease: Photosensitivity of skin
Photosensitivity of skin 		91 0 1 2.0E-03 0 0
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology 		86 0 1 2.0E-03 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 0 1 2.0E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 2.0E-03 0 0
CUI: C0221260
Disease: Dystrophia unguium
Dystrophia unguium 		81 0 1 2.0E-03 0 0
CUI: C0241726
Disease: Delayed ability to walk
Delayed ability to walk 		77 0 1 2.0E-03 0 0
CUI: C0240953
Disease: Winged scapula
Winged scapula 		73 0 1 2.0E-03 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 0 1 2.0E-03 0 0
CUI: C3203547
Disease: Axial spondyloarthritis
Axial spondyloarthritis 		67 0 1 2.1E-03 0 0
CUI: C3501844
Disease: Familial Nonmedullary Thyroid Cancer
Familial Nonmedullary Thyroid Cancer 		66 0 1 2.1E-03 0 0
CUI: C1855710
Disease: Bone marrow hypocellularity
Bone marrow hypocellularity 		64 0 1 2.1E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 1 2.1E-03 0 0
CUI: C4722327
Disease: PROSTATE CANCER, HEREDITARY, 1
PROSTATE CANCER, HEREDITARY, 1 		62 0 1 2.1E-03 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		61 0 1 2.1E-03 0 0
CUI: C3277226
Disease: Restrictive ventilatory defect
Restrictive ventilatory defect 		61 0 1 2.1E-03 0 0
CUI: C0426817
Disease: Short ribs
Short ribs 		60 0 1 2.1E-03 0 0