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: C1849923
Disease: Generalized hypopigmentation
Generalized hypopigmentation 		23 0 1 3.2E-04 0 0
CUI: C1842180
Disease: CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder)
CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder) 		22 0 1 3.2E-04 0 0
CUI: C1856660
Disease: Abnormality of the helix
Abnormality of the helix 		21 0 1 3.2E-04 0 0
CUI: C0079153
Disease: Hyperkeratosis, Epidermolytic
Hyperkeratosis, Epidermolytic 		20 0 1 3.2E-04 0 0
CUI: C0266231
Disease: Ectopic anus
Ectopic anus 		20 0 1 3.2E-04 0 0
CUI: C0751779
Disease: Action Myoclonus-Renal Failure Syndrome
Action Myoclonus-Renal Failure Syndrome 		20 0 1 3.2E-04 0 0
CUI: C3887496
Disease: Oligodactyly
Oligodactyly 		20 0 1 3.2E-04 0 0
CUI: C0152233
Disease: Congenital ankyloblepharon
Congenital ankyloblepharon 		18 0 1 3.2E-04 0 0
CUI: C0339182
Disease: Ankyloblepharon
Ankyloblepharon 		18 0 1 3.2E-04 0 0
CUI: C1398522
Disease: Cleft palate and bilateral cleft lip
Cleft palate and bilateral cleft lip 		18 0 1 3.2E-04 0 0
CUI: C1740801
Disease: Exaggerated startle response
Exaggerated startle response 		18 0 1 3.2E-04 0 0
CUI: C0751776
Disease: Atypical Inclusion-Body Disease
Atypical Inclusion-Body Disease 		17 0 1 3.2E-04 0 0
CUI: C0751777
Disease: Familial Progressive Myoclonic Epilepsy
Familial Progressive Myoclonic Epilepsy 		17 0 1 3.2E-04 0 0
CUI: C0751780
Disease: Biotin-Responsive Encephalopathy
Biotin-Responsive Encephalopathy 		17 0 1 3.2E-04 0 0
CUI: C0751782
Disease: May-White Syndrome
May-White Syndrome 		17 0 1 3.2E-04 0 0
CUI: C1850259
Disease: Short tibia
Short tibia 		17 0 1 3.2E-04 0 0
CUI: C2936694
Disease: Swyer Syndrome
Swyer Syndrome 		17 0 1 3.2E-04 0 0
CUI: C0302254
Disease: Juvenile cataract
Juvenile cataract 		16 0 1 3.2E-04 0 0
CUI: C2931850
Disease: Aase Smith syndrome 2
Aase Smith syndrome 2 		16 0 1 3.2E-04 0 0
CUI: C0021603
Disease: Sleep Initiation and Maintenance Disorders
Sleep Initiation and Maintenance Disorders 		15 0 1 3.2E-04 0 0
CUI: C1843505
Disease: Degeneration of anterior horn cells
Degeneration of anterior horn cells 		15 0 1 3.2E-04 0 0
CUI: C1853171
Disease: Multiple prenatal fractures
Multiple prenatal fractures 		15 0 1 3.2E-04 0 0
CUI: C3536734
Disease: Hypoplastic pelvis
Hypoplastic pelvis 		15 0 1 3.2E-04 0 0
CUI: C4023721
Disease: Abnormal hair pattern
Abnormal hair pattern 		15 0 1 3.2E-04 0 0
CUI: C0004681
Disease: Bagassosis
Bagassosis 		14 0 1 3.2E-04 0 0