Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Mental Retardation, X-Linked, Syndromic, Christianson Type
6 0 1 0.17 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
Shortening of all distal phalanges of the fingers
40 0 1 2.5E-02 0 0
CUI: C4023687
Disease: EEG with multifocal slow activity
EEG with multifocal slow activity
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: C1857704
Disease: Abnormal myelination
Abnormal myelination
49 0 1 2.0E-02 0 0
CUI: C1858036
Disease: Periorbital fullness
Periorbital fullness
57 0 1 1.8E-02 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum
63 0 1 1.6E-02 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology
70 0 1 1.4E-02 0 0
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure
73 0 1 1.4E-02 0 0
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia
77 0 1 1.3E-02 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 1.2E-02 0 0
CUI: C0003537
Disease: Aphasia
Aphasia
86 0 1 1.2E-02 0 0
CUI: C0013132
Disease: Drooling
Drooling
95 0 1 1.1E-02 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities
112 0 1 8.9E-03 0 0
CUI: C0034194
Disease: Pyloric Stenosis
Pyloric Stenosis
121 0 1 8.3E-03 0 0
CUI: C0035304
Disease: Retinal Degeneration
Retinal Degeneration
125 0 1 8.0E-03 0 0
CUI: C0426429
Disease: Broad nasal tip
Broad nasal tip
125 0 1 8.0E-03 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision
127 0 1 7.9E-03 0 0
CUI: C0239174
Disease: Late tooth eruption
Late tooth eruption
139 0 1 7.2E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady
143 0 1 7.0E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion
145 0 1 6.9E-03 0 0