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: C0745730
Disease: Multiple lipomata
Multiple lipomata
38 0 13 9.2E-02 0 0
DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
38 0 13 9.2E-02 0 0
CUI: C0003537
Disease: Aphasia
Aphasia
86 0 17 9.1E-02 0 0
CUI: C0020757
Disease: Ichthyoses
Ichthyoses
194 0 26 9.1E-02 0 0
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes
31 0 12 8.8E-02 0 0
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies
121 0 19 8.7E-02 0 0
CUI: C4022012
Disease: Death in early adulthood
Death in early adulthood
46 0 13 8.7E-02 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment
136 0 20 8.6E-02 0 0
CUI: C0234428
Disease: Disturbance of consciousness
Disturbance of consciousness
35 0 12 8.6E-02 0 0
CUI: C4025821
Disease: Anterior hypopituitarism
Anterior hypopituitarism
48 0 13 8.6E-02 0 0
CUI: C0242698
Disease: Ventricular Dysfunction, Left
Ventricular Dysfunction, Left
88 0 16 8.5E-02 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
312 0 33 8.3E-02 0 0
CUI: C0020626
Disease: Hypoparathyroidism
Hypoparathyroidism
92 15 16 8.3E-02 1 2.3E-02
CUI: C1384666
Disease: hearing impairment
hearing impairment
740 337 65 8.2E-02 4 1.1E-02
Congenital sensorineural hearing loss
68 0 14 8.2E-02 0 0
CUI: C1855285
Disease: Protruding ear
Protruding ear
152 0 20 8.0E-02 0 0
CUI: C0021843
Disease: Intestinal Obstruction
Intestinal Obstruction
87 0 15 7.9E-02 0 0
CUI: C0018021
Disease: Goiter
Goiter
142 0 19 7.9E-02 0 0
CUI: C3810365
Disease: Central visual impairment
Central visual impairment
158 0 20 7.8E-02 0 0
CUI: C0149793
Disease: Amaurosis Fugax
Amaurosis Fugax
49 0 12 7.8E-02 0 0
CUI: C1848641
Disease: Profound sensorineural hearing loss
Profound sensorineural hearing loss
22 0 10 7.8E-02 0 0
CUI: C0424448
Disease: Mask-like facies
Mask-like facies
64 0 13 7.7E-02 0 0
CUI: C1866934
Disease: Reduced tendon reflexes
Reduced tendon reflexes
121 0 17 7.7E-02 0 0
CUI: C1836735
Disease: hypopigmented skin patch
hypopigmented skin patch
123 0 17 7.6E-02 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 20 7.5E-02 0 0