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: C0000921
Disease: Accidental Falls
Accidental Falls
22 0 1 4.5E-02 0 0
CUI: C0003486
Disease: Aortic Aneurysm
Aortic Aneurysm
278 0 1 3.6E-03 0 0
CUI: C0003742
Disease: Arcus Senilis
Arcus Senilis
13 0 1 7.7E-02 0 0
CUI: C0004158
Disease: Athetosis
Athetosis
39 0 1 2.6E-02 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
441 0 1 2.3E-03 0 0
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
285 0 1 3.5E-03 0 0
CUI: C0009782
Disease: Connective Tissue Diseases
Connective Tissue Diseases
188 0 1 5.3E-03 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity
113 0 1 8.8E-03 0 0
CUI: C0010495
Disease: Cutis Laxa
Cutis Laxa
70 0 1 1.4E-02 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism
1261 0 1 7.9E-04 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 2.1E-03 0 0
Pathological accumulation of air in tissues
69 0 1 1.4E-02 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
842 0 1 1.2E-03 0 0
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
1037 0 1 9.6E-04 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot
285 0 1 3.5E-03 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
272 0 1 3.7E-03 0 0
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease
446 0 1 2.2E-03 0 0
Sensorineural Hearing Loss (disorder)
783 0 1 1.3E-03 0 0
CUI: C0019270
Disease: Hernia
Hernia
136 0 1 7.4E-03 0 0
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal
225 0 1 4.4E-03 0 0
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
590 0 1 1.7E-03 0 0
CUI: C0023222
Disease: Pain in lower limb
Pain in lower limb
31 0 1 3.2E-02 0 0
CUI: C0025202
Disease: melanoma
melanoma
3087 0 1 3.2E-04 0 0
CUI: C0025517
Disease: Metabolic Diseases
Metabolic Diseases
945 0 1 1.1E-03 0 0
CUI: C0025958
Disease: Microcephaly
Microcephaly
1064 0 1 9.4E-04 0 0