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: C0280252
Disease: stage, colon cancer
stage, colon cancer 		0 2 0 0 1 3.0E-02
CUI: C1290073
Disease: Acute mucositis
Acute mucositis 		0 1 0 0 1 3.1E-02
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1 		0 10 0 0 1 2.4E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 2.9E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		433 0 1 1.9E-03 0 0
CUI: C0037369
Disease: Smoking
Smoking 		391 0 1 2.0E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 2.7E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		261 0 1 2.8E-03 0 0
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 2 3.0E-03 0 0
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		228 0 1 3.1E-03 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia 		226 0 1 3.1E-03 0 0
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal 		225 0 1 3.1E-03 0 0
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 3.1E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 3 3.2E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 0 1 3.2E-03 0 0
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion 		211 0 1 3.2E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 3.3E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		205 0 1 3.3E-03 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		198 0 1 3.4E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia 		191 0 1 3.5E-03 0 0
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		473 0 2 3.5E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 3.5E-03 0 0
CUI: C0235991
Disease: Small for gestational age (disorder)
Small for gestational age (disorder) 		181 0 1 3.6E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 3.6E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 1 3.7E-03 0 0