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: C0233702
Disease: Algophobia
Algophobia
0 4 0 0 1 2.3E-03
CUI: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant
0 2 0 0 2 4.6E-03
CUI: C0518964
Disease: BRONCHIAL ADENOCARCINOMA
BRONCHIAL ADENOCARCINOMA
0 1 0 0 1 2.3E-03
CUI: C1861825
Disease: CATARACT, POSTERIOR POLAR, 1
CATARACT, POSTERIOR POLAR, 1
0 4 0 0 1 2.3E-03
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement
0 149 0 0 1 1.7E-03
CUI: C0266483
Disease: Pachygyria
Pachygyria
129 0 1 1.5E-03 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation
98 0 1 1.6E-03 0 0
CUI: C1837463
Disease: Narrow face
Narrow face
87 0 1 1.6E-03 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment
86 0 1 1.6E-03 0 0
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen
80 0 1 1.6E-03 0 0
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance
76 0 1 1.6E-03 0 0
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic
75 0 1 1.6E-03 0 0
CUI: C0409338
Disease: Flexion contracture - elbow
Flexion contracture - elbow
73 0 1 1.6E-03 0 0
CUI: C0426415
Disease: Large nose
Large nose
70 0 1 1.6E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
63 0 1 1.7E-03 0 0
CUI: C0004144
Disease: Atelectasis
Atelectasis
62 0 1 1.7E-03 0 0
CUI: C0231687
Disease: Spastic gait
Spastic gait
62 0 1 1.7E-03 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly
62 0 1 1.7E-03 0 0
CUI: C0009024
Disease: Clonus
Clonus
60 0 1 1.7E-03 0 0
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect
59 0 1 1.7E-03 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance
57 0 1 1.7E-03 0 0
CUI: C4316870
Disease: Abnormality of the eye
Abnormality of the eye
56 0 1 1.7E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus
55 0 1 1.7E-03 0 0
Adverse effects, not elsewhere classified
55 0 1 1.7E-03 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem
55 0 1 1.7E-03 0 0