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: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0 350 0 0 1 2.7E-03
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
0 14 0 0 1 3.3E-02
CUI: C0002886
Disease: Anemia, Macrocytic
Anemia, Macrocytic
0 1 0 0 1 5.9E-02
CUI: C0003635
Disease: Apraxias
Apraxias
0 7 0 0 1 4.3E-02
CUI: C0009024
Disease: Clonus
Clonus
0 4 0 0 1 5.0E-02
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0 39 0 0 1 1.8E-02
CUI: C0014877
Disease: Esotropia
Esotropia
0 39 0 0 1 1.8E-02
CUI: C0015310
Disease: Exotropia
Exotropia
0 21 0 0 2 5.6E-02
CUI: C0016202
Disease: Flatfoot
Flatfoot
0 38 0 0 1 1.9E-02
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis
0 17 0 0 1 3.0E-02
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
0 77 0 0 1 1.1E-02
CUI: C0020608
Disease: Hypodontia
Hypodontia
0 15 0 0 1 3.2E-02
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia
0 15 0 0 1 3.2E-02
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0 245 0 0 1 3.8E-03
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
0 89 0 0 1 9.5E-03
CUI: C0023882
Disease: Little's Disease
Little's Disease
0 6 0 0 1 4.5E-02
CUI: C0025362
Disease: Mental Retardation
Mental Retardation
0 36 0 0 1 1.9E-02
CUI: C0025990
Disease: Micrognathism
Micrognathism
0 52 0 0 1 1.5E-02
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
0 93 0 0 1 9.2E-03
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0 240 0 0 2 7.8E-03
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
0 21 0 0 1 2.7E-02
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
0 579 0 0 3 5.1E-03
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
0 39 0 0 2 3.7E-02
CUI: C0027080
Disease: Myoglobinuria
Myoglobinuria
0 1 0 0 1 5.9E-02
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy
0 34 0 0 1 2.0E-02