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: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
308 0 2 6.5E-03 0 0
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease
129 0 2 1.6E-02 0 0
CUI: C0019572
Disease: Hirsutism
Hirsutism
87 0 2 2.3E-02 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
207 0 2 9.7E-03 0 0
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior
120 0 2 1.7E-02 0 0
CUI: C0022548
Disease: Keloid
Keloid
5 0 2 0.40 0 0
CUI: C0023234
Disease: Legg-Calve-Perthes Disease
Legg-Calve-Perthes Disease
21 0 2 9.5E-02 0 0
CUI: C0023418
Disease: leukemia
leukemia
36 0 2 5.6E-02 0 0
CUI: C0024636
Disease: Malocclusion
Malocclusion
93 0 2 2.2E-02 0 0
CUI: C0025149
Disease: Medulloblastoma
Medulloblastoma
26 0 2 7.7E-02 0 0
CUI: C0025958
Disease: Microcephaly
Microcephaly
855 0 2 2.3E-03 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism
574 0 2 3.5E-03 0 0
CUI: C0026034
Disease: Microstomia
Microstomia
171 0 2 1.2E-02 0 0
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation
269 0 1 3.7E-03 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
196 0 1 5.1E-03 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
954 0 2 2.1E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
491 0 1 2.0E-03 0 0
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip
58 0 1 1.7E-02 0 0
CUI: C0033377
Disease: Ptosis
Ptosis
558 0 2 3.6E-03 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
773 0 2 2.6E-03 0 0
CUI: C0036572
Disease: Seizures
Seizures
1292 0 2 1.5E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior
134 0 2 1.5E-02 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder
150 0 2 1.3E-02 0 0
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
42 0 1 2.3E-02 0 0
CUI: C0039075
Disease: Syndactyly
Syndactyly
77 0 2 2.6E-02 0 0