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: C1836038
Disease: Poor head control
Poor head control
162 0 1 3.0E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
160 0 1 3.0E-03 0 0
CUI: C0240063
Disease: Coloboma of iris
Coloboma of iris
153 0 1 3.1E-03 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris
148 0 1 3.1E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency
148 0 1 3.1E-03 0 0
Muscular Dystrophy, Facioscapulohumeral
143 0 1 3.2E-03 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial
142 0 1 3.2E-03 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition
140 0 1 3.2E-03 0 0
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum
138 0 1 3.2E-03 0 0
Platelet Component Distribution Width Measurement
134 0 1 3.3E-03 0 0
CUI: C1849089
Disease: Broad forehead
Broad forehead
133 0 1 3.3E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
131 0 1 3.3E-03 0 0
CUI: C1837404
Disease: High, narrow palate
High, narrow palate
129 0 1 3.3E-03 0 0
CUI: C0039075
Disease: Syndactyly
Syndactyly
127 0 1 3.3E-03 0 0
CUI: C0240543
Disease: Bulbous nose
Bulbous nose
123 0 1 3.4E-03 0 0
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly
123 0 1 3.4E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia
121 0 1 3.4E-03 0 0
CUI: C1866934
Disease: Reduced tendon reflexes
Reduced tendon reflexes
121 0 1 3.4E-03 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly
120 0 1 3.4E-03 0 0
CUI: C0431380
Disease: Cortical Dysplasia
Cortical Dysplasia
118 0 1 3.4E-03 0 0
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay
118 0 1 3.4E-03 0 0
CUI: C0576093
Disease: Knee joint valgus deformity
Knee joint valgus deformity
117 0 1 3.4E-03 0 0
CUI: C1842876
Disease: Depressed nasal ridge
Depressed nasal ridge
117 0 1 3.4E-03 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 1 3.5E-03 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities
115 0 1 3.5E-03 0 0