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: C0043207
Disease: Wolfram Syndrome
Wolfram Syndrome 		0 7 0 0 2 1.0E-01
CUI: C0085932
Disease: Bullous Dermatitis
Bullous Dermatitis 		0 1 0 0 1 6.7E-02
CUI: C2677096
Disease: SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11
SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11 		0 1 0 0 1 6.7E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity 		430 0 1 1.9E-03 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy 		305 0 1 2.4E-03 0 0
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		271 0 1 2.7E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche 		267 0 1 2.7E-03 0 0
CUI: C1305855
Disease: Body mass index
Body mass index 		1014 0 3 2.7E-03 0 0
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		265 0 1 2.7E-03 0 0
CUI: C0003578
Disease: Apnea
Apnea 		262 0 1 2.7E-03 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability 		251 0 1 2.8E-03 0 0
CUI: C0489786
Disease: Height
Height 		249 0 1 2.8E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 2.9E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 3.0E-03 0 0
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		565 0 2 3.0E-03 0 0
CUI: C1853242
Disease: Midface retrusion
Midface retrusion 		228 0 1 3.0E-03 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal 		227 0 1 3.0E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 1 3.1E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 0 1 3.1E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 3.1E-03 0 0
CUI: C0239676
Disease: High forehead
High forehead 		211 0 1 3.2E-03 0 0
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		208 0 1 3.2E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 0 1 3.2E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry 		206 0 1 3.2E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		205 0 1 3.2E-03 0 0