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: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia
100 0 1 2.3E-03 0 0
CUI: C4551488
Disease: Bifid uvula
Bifid uvula
97 0 1 2.4E-03 0 0
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
96 0 1 2.4E-03 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls
94 0 1 2.4E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
90 0 1 2.4E-03 0 0
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
89 0 1 2.4E-03 0 0
CUI: C0424711
Disease: Orbital separation diminished
Orbital separation diminished
89 0 1 2.4E-03 0 0
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
89 0 1 2.4E-03 0 0
Premature coronary artery atherosclerosis
87 0 1 2.4E-03 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment
86 0 1 2.4E-03 0 0
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology
86 0 1 2.4E-03 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis
85 0 1 2.4E-03 0 0
Respiratory insufficiency due to muscle weakness
85 0 1 2.4E-03 0 0
CUI: C0751713
Disease: Inclusion Body Myopathy, Sporadic
Inclusion Body Myopathy, Sporadic
84 0 1 2.4E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea
82 0 1 2.4E-03 0 0
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
82 0 1 2.4E-03 0 0
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
82 0 1 2.4E-03 0 0
CUI: C0020758
Disease: Congenital ichthyosis
Congenital ichthyosis
80 0 1 2.5E-03 0 0
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome
80 0 1 2.5E-03 0 0
CUI: C0015310
Disease: Exotropia
Exotropia
78 0 1 2.5E-03 0 0
CUI: C0236733
Disease: Amphetamine-Related Disorders
Amphetamine-Related Disorders
78 0 1 2.5E-03 0 0
CUI: C1834405
Disease: Nail dysplasia
Nail dysplasia
78 0 1 2.5E-03 0 0
CUI: C1839364
Disease: Progressive visual loss
Progressive visual loss
77 0 1 2.5E-03 0 0
NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9
77 0 1 2.5E-03 0 0
CUI: C0012569
Disease: Diplopia
Diplopia
75 0 1 2.5E-03 0 0