Source: INFERRED ×
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: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		33 190 1 3.0E-02 1 5.0E-03
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm 		26 152 1 3.8E-02 1 6.1E-03
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		55 94 1 1.8E-02 2 1.9E-02
CUI: C0038379
Disease: Strabismus
Strabismus 		682 85 1 1.5E-03 1 1.0E-02
CUI: C0280630
Disease: Uterine Carcinosarcoma
Uterine Carcinosarcoma 		12 80 1 8.3E-02 1 1.1E-02
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		590 77 1 1.7E-03 2 2.3E-02
CUI: C0239234
Disease: Low set ears
Low set ears 		489 64 1 2.0E-03 1 1.3E-02
CUI: C0025990
Disease: Micrognathism
Micrognathism 		574 52 1 1.7E-03 1 1.6E-02
CUI: C0423110
Disease: Downward slant of palpebral fissure
Downward slant of palpebral fissure 		391 49 1 2.6E-03 2 3.3E-02
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		42 47 1 2.4E-02 8 0.15
CUI: C1854301
Disease: Motor delay
Motor delay 		381 34 1 2.6E-03 1 2.2E-02
CUI: C2931196
Disease: Craniofacial dysostosis type 1
Craniofacial dysostosis type 1 		3 34 1 0.33 10 0.27
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		107 33 1 9.3E-03 3 7.0E-02
CUI: C0265269
Disease: Lacrimoauriculodentodigital syndrome
Lacrimoauriculodentodigital syndrome 		3 32 1 0.33 8 0.22
CUI: C0014170
Disease: Endometrial Neoplasms
Endometrial Neoplasms 		14 30 1 7.1E-02 3 7.5E-02
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		2 30 1 0.50 9 0.26
CUI: C0175699
Disease: Saethre-Chotzen Syndrome
Saethre-Chotzen Syndrome 		3 29 1 0.33 8 0.24
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		150 25 1 6.7E-03 1 2.7E-02
CUI: C1837260
Disease: Prominent forehead
Prominent forehead 		159 25 1 6.3E-03 1 2.7E-02
CUI: C0431447
Disease: Synophrys
Synophrys 		111 23 1 9.0E-03 1 2.9E-02
CUI: C0795998
Disease: JACKSON-WEISS SYNDROME
JACKSON-WEISS SYNDROME 		2 15 1 0.50 8 0.40
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		1 14 1 1.00 9 0.50
CUI: C1867131
Disease: Broad hallux
Broad hallux 		48 14 1 2.1E-02 1 3.8E-02
CUI: C1306710
Disease: Facial asymmetry
Facial asymmetry 		108 13 1 9.3E-03 1 4.0E-02
CUI: C1849089
Disease: Broad forehead
Broad forehead 		133 13 1 7.5E-03 1 4.0E-02