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: C0011848
Disease: Diabetes Insipidus
Diabetes Insipidus
35 0 1 2.9E-02 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism
1039 0 1 9.6E-04 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
470 0 1 2.1E-03 0 0
CUI: C0013528
Disease: Echolalia
Echolalia
38 0 1 2.6E-02 0 0
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia
74 0 1 1.4E-02 0 0
CUI: C0014850
Disease: Esophageal Atresia
Esophageal Atresia
24 0 1 4.2E-02 0 0
CUI: C0015300
Disease: Exophthalmos
Exophthalmos
200 0 1 5.0E-03 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
734 0 1 1.4E-03 0 0
CUI: C0015672
Disease: Fatigue
Fatigue
340 0 1 2.9E-03 0 0
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
432 0 1 2.3E-03 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot
282 0 1 3.5E-03 0 0
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
33 0 1 3.0E-02 0 0
CUI: C0018418
Disease: Gynecomastia
Gynecomastia
90 0 1 1.1E-02 0 0
Sensorineural Hearing Loss (disorder)
622 0 1 1.6E-03 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
250 0 1 4.0E-03 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
308 0 1 3.2E-03 0 0
CUI: C0018916
Disease: Hemangioma
Hemangioma
69 0 1 1.4E-02 0 0
CUI: C0018989
Disease: Hemiparesis
Hemiparesis
83 0 1 1.2E-02 0 0
CUI: C0018991
Disease: Hemiplegia
Hemiplegia
32 0 1 3.1E-02 0 0
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal
208 0 1 4.8E-03 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
297 0 1 3.4E-03 0 0
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis
184 0 1 5.4E-03 0 0
CUI: C0020488
Disease: Hypernatremia
Hypernatremia
6 0 1 0.17 0 0
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
590 0 1 1.7E-03 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia
184 0 1 5.4E-03 0 0