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: C0523677
Disease: Glycine measurement
Glycine measurement 		32 0 1 2.9E-02 0 0
CUI: C1292772
Disease: Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative
Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative 		32 0 1 2.9E-02 0 0
CUI: C4287589
Disease: Serous Tubal Intraepithelial Carcinoma
Serous Tubal Intraepithelial Carcinoma 		33 0 1 2.8E-02 0 0
CUI: C3853041
Disease: Severe Congenital Microcephaly
Severe Congenital Microcephaly 		35 0 1 2.6E-02 0 0
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		116 0 3 2.6E-02 0 0
CUI: C4012968
Disease: Mild global developmental delay
Mild global developmental delay 		36 0 1 2.6E-02 0 0
CUI: C1857656
Disease: Prematurely aged appearance
Prematurely aged appearance 		40 0 1 2.3E-02 0 0
CUI: C1956147
Disease: Microlissencephaly
Microlissencephaly 		40 0 1 2.3E-02 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		149 0 3 2.0E-02 0 0
CUI: C1855285
Disease: Protruding ear
Protruding ear 		152 0 3 2.0E-02 0 0
CUI: C1865037
Disease: Cone-shaped epiphysis
Cone-shaped epiphysis 		49 0 1 1.9E-02 0 0
CUI: C2216702
Disease: malignant neoplasm of breast staging
malignant neoplasm of breast staging 		49 0 1 1.9E-02 0 0
CUI: C0587248
Disease: Costello syndrome (disorder)
Costello syndrome (disorder) 		50 0 1 1.9E-02 0 0
CUI: C2921627
Disease: Clinically isolated syndrome
Clinically isolated syndrome 		54 0 1 1.8E-02 0 0
CUI: C3160889
Disease: Node-negative breast cancer
Node-negative breast cancer 		54 0 1 1.8E-02 0 0
CUI: C0027654
Disease: Embryonal Neoplasm
Embryonal Neoplasm 		57 0 1 1.7E-02 0 0
CUI: C0339467
Disease: Proliferative retinopathy
Proliferative retinopathy 		57 0 1 1.7E-02 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 3 1.7E-02 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation 		58 0 1 1.6E-02 0 0
CUI: C1840069
Disease: Sandal gap
Sandal gap 		62 0 1 1.5E-02 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia 		197 0 3 1.5E-02 0 0
CUI: C1333762
Disease: Gastric Cardia Adenocarcinoma
Gastric Cardia Adenocarcinoma 		65 0 1 1.5E-02 0 0
CUI: C4024202
Disease: Reduced number of teeth
Reduced number of teeth 		67 0 1 1.4E-02 0 0
CUI: C0240538
Disease: Convex nasal ridge
Convex nasal ridge 		69 0 1 1.4E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 3 1.4E-02 0 0