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: C1845181
Disease: MENTAL RETARDATION, X-LINKED 78
MENTAL RETARDATION, X-LINKED 78
3 0 1 0.33 0 0
Abnormal tracheobronchial morphology
4 0 1 0.25 0 0
CUI: C1844007
Disease: Corticospinal tract hypoplasia
Corticospinal tract hypoplasia
5 0 1 0.20 0 0
EEG with centrotemporal focal spike waves
5 0 1 0.20 0 0
CUI: C0175713
Disease: Aicardi's syndrome
Aicardi's syndrome
7 0 1 0.14 0 0
CUI: C0860609
Disease: Inappropriate crying
Inappropriate crying
8 0 1 0.12 0 0
CUI: C3854333
Disease: Narrowing
Narrowing
8 0 1 0.12 0 0
CUI: C4023014
Disease: Stereotypical hand wringing
Stereotypical hand wringing
8 0 1 0.12 0 0
CUI: C2748652
Disease: Large face
Large face
11 0 1 9.1E-02 0 0
CUI: C1849538
Disease: Delayed eruption of primary teeth
Delayed eruption of primary teeth
14 0 1 7.1E-02 0 0
CUI: C0085426
Disease: Gram-Positive Bacterial Infections
Gram-Positive Bacterial Infections
17 0 1 5.9E-02 0 0
CUI: C1840382
Disease: Abnormality of the ureter
Abnormality of the ureter
19 0 1 5.3E-02 0 0
CUI: C0034880
Disease: Hyperacusis
Hyperacusis
20 0 1 5.0E-02 0 0
CUI: C0006325
Disease: Bruxism
Bruxism
24 0 1 4.2E-02 0 0
CUI: C4021620
Disease: Clinodactyly of the 2nd toe
Clinodactyly of the 2nd toe
32 0 1 3.1E-02 0 0
Moderate sensorineural hearing impairment
34 0 1 2.9E-02 0 0
CUI: C1846151
Disease: Widened subarachnoid space
Widened subarachnoid space
35 0 1 2.9E-02 0 0
Mild neurosensory hearing impairment
35 0 1 2.9E-02 0 0
CUI: C0150080
Disease: Social Communication Disorder
Social Communication Disorder
40 0 1 2.5E-02 0 0
CUI: C0266039
Disease: Taurodontism
Taurodontism
40 0 1 2.5E-02 0 0
CUI: C4020968
Disease: Abnormal localization of kidney
Abnormal localization of kidney
40 0 1 2.5E-02 0 0
Shortening of all distal phalanges of the fingers
40 0 1 2.5E-02 0 0
CUI: C1837522
Disease: Impaired pain sensation
Impaired pain sensation
41 0 1 2.4E-02 0 0
CUI: C2931498
Disease: Mental Retardation, X-Linked 1
Mental Retardation, X-Linked 1
45 0 1 2.2E-02 0 0
CUI: C0795864
Disease: Smith-Magenis syndrome
Smith-Magenis syndrome
47 0 1 2.1E-02 0 0