Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Diabetic peripheral neuropathic pain
0 1 0 0 1 1.6E-02
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans
0 9 0 0 1 1.4E-02
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate
169 0 1 1.3E-03 0 0
CUI: C1836543
Disease: Thick vermilion border
Thick vermilion border
95 0 1 1.4E-03 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate
87 0 1 1.4E-03 0 0
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion
79 0 1 1.4E-03 0 0
CUI: C3554617
Disease: Adducted thumb
Adducted thumb
74 0 1 1.4E-03 0 0
CUI: C0426848
Disease: Sacral dimple
Sacral dimple
69 0 1 1.5E-03 0 0
CUI: C1855340
Disease: Bowing of the long bones
Bowing of the long bones
63 0 1 1.5E-03 0 0
CUI: C0234378
Disease: Static Tremor
Static Tremor
62 0 1 1.5E-03 0 0
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
62 0 1 1.5E-03 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement
62 0 1 1.5E-03 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly
62 0 1 1.5E-03 0 0
CUI: C4722327
Disease: PROSTATE CANCER, HEREDITARY, 1
PROSTATE CANCER, HEREDITARY, 1
62 0 1 1.5E-03 0 0
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence
60 0 1 1.5E-03 0 0
CUI: C0426817
Disease: Short ribs
Short ribs
60 0 1 1.5E-03 0 0
Fatigable weakness of respiratory muscles
60 0 1 1.5E-03 0 0
CUI: C0002902
Disease: Anencephaly
Anencephaly
59 0 1 1.5E-03 0 0
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation
59 0 1 1.5E-03 0 0
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia
59 0 1 1.5E-03 0 0
CUI: C1857640
Disease: Decreased nerve conduction velocity
Decreased nerve conduction velocity
58 0 1 1.5E-03 0 0
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval
57 0 1 1.5E-03 0 0
CUI: C1866730
Disease: Rhizomelia
Rhizomelia
57 0 1 1.5E-03 0 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy
56 0 1 1.5E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus
55 0 1 1.5E-03 0 0