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: C2931498
Disease: Mental Retardation, X-Linked 1
Mental Retardation, X-Linked 1
45 0 37 0.25 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive
172 0 49 0.19 0 0
CUI: C4021620
Disease: Clinodactyly of the 2nd toe
Clinodactyly of the 2nd toe
32 0 26 0.18 0 0
Shortening of all distal phalanges of the fingers
40 0 27 0.18 0 0
Moderate sensorineural hearing impairment
34 0 26 0.17 0 0
CUI: C1846151
Disease: Widened subarachnoid space
Widened subarachnoid space
35 0 26 0.17 0 0
Mild neurosensory hearing impairment
35 0 26 0.17 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities
112 0 34 0.16 0 0
CUI: C1858036
Disease: Periorbital fullness
Periorbital fullness
57 0 26 0.15 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 29 0.15 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum
63 0 26 0.15 0 0
CUI: C0013132
Disease: Drooling
Drooling
95 0 30 0.15 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation
505 98 82 0.15 3 2.8E-02
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure
73 0 27 0.14 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
251 0 49 0.14 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion
145 0 33 0.13 0 0
CUI: C0426429
Disease: Broad nasal tip
Broad nasal tip
125 0 29 0.12 0 0
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability
429 74 60 0.12 1 1.2E-02
CUI: C0042024
Disease: Urinary Incontinence
Urinary Incontinence
151 0 30 0.11 0 0
CUI: C0239174
Disease: Late tooth eruption
Late tooth eruption
139 0 28 0.11 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior
261 0 40 0.11 0 0
CUI: C0034194
Disease: Pyloric Stenosis
Pyloric Stenosis
121 0 26 0.11 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance
65 0 20 0.11 0 0
CUI: C0221355
Disease: Macrocephaly
Macrocephaly
367 0 49 0.11 0 0
Mental Retardation, X-Linked Nonsyndromic
16 0 15 0.11 0 0