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: C0266037
Disease: Peg-shaped teeth
Peg-shaped teeth
17 0 1 3.5E-04 0 0
CUI: C4021626
Disease: Lethal skeletal dysplasia
Lethal skeletal dysplasia
17 0 1 3.5E-04 0 0
CUI: C1832338
Disease: Axonal loss
Axonal loss
16 0 1 3.5E-04 0 0
CUI: C1837899
Disease: Type I transferrin isoform profile
Type I transferrin isoform profile
16 0 1 3.5E-04 0 0
CUI: C2931850
Disease: Aase Smith syndrome 2
Aase Smith syndrome 2
16 0 1 3.5E-04 0 0
CUI: C4293708
Disease: Recurrent paroxysmal headache
Recurrent paroxysmal headache
16 0 1 3.5E-04 0 0
CUI: C0684219
Disease: Myokymia
Myokymia
15 0 1 3.5E-04 0 0
CUI: C0730303
Disease: Capillary hemangioma of retina
Capillary hemangioma of retina
15 0 1 3.5E-04 0 0
CUI: C2699746
Disease: Syndactyly, type 2
Syndactyly, type 2
15 0 1 3.5E-04 0 0
Abnormal isoelectric focusing of serum transferrin
15 0 1 3.5E-04 0 0
CUI: C4022998
Disease: Arachnoid hemangiomatosis
Arachnoid hemangiomatosis
15 0 1 3.5E-04 0 0
CUI: C4023786
Disease: Elevated levels of phytanic acid
Elevated levels of phytanic acid
15 0 1 3.5E-04 0 0
CUI: C0232608
Disease: Nasal regurgitation
Nasal regurgitation
14 0 1 3.5E-04 0 0
CUI: C0240116
Disease: Hyperactive patellar reflex
Hyperactive patellar reflex
14 0 1 3.5E-04 0 0
CUI: C0473133
Disease: Protracted diarrhea
Protracted diarrhea
14 0 1 3.5E-04 0 0
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone
14 0 1 3.5E-04 0 0
CUI: C1273957
Disease: Upper limb spasticity
Upper limb spasticity
14 0 1 3.5E-04 0 0
CUI: C1303007
Disease: Brushfield spots
Brushfield spots
14 0 1 3.5E-04 0 0
CUI: C1855514
Disease: Severe failure to thrive
Severe failure to thrive
14 0 1 3.5E-04 0 0
CUI: C1856408
Disease: Infantile encephalopathy
Infantile encephalopathy
14 0 1 3.5E-04 0 0
Fatigable weakness of bulbar muscles
14 0 1 3.5E-04 0 0
CUI: C0751594
Disease: Zellweger-Like Syndrome
Zellweger-Like Syndrome
13 0 1 3.5E-04 0 0
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction
13 0 1 3.5E-04 0 0
CUI: C1856118
Disease: Prominent nasal tip
Prominent nasal tip
13 0 1 3.5E-04 0 0
CUI: C3806510
Disease: Horizontal ribs
Horizontal ribs
13 0 1 3.5E-04 0 0