Source: ALL
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: C4021620
Disease: Clinodactyly of the 2nd toe
Clinodactyly of the 2nd toe 		32 0 32 0.38 0 0
CUI: C4021608
Disease: Shortening of all distal phalanges of the fingers
Shortening of all distal phalanges of the fingers 		40 0 34 0.37 0 0
CUI: C4024664
Disease: Moderate sensorineural hearing impairment
Moderate sensorineural hearing impairment 		34 0 32 0.37 0 0
CUI: C1846151
Disease: Widened subarachnoid space
Widened subarachnoid space 		35 0 32 0.36 0 0
CUI: C4021538
Disease: Mild neurosensory hearing impairment
Mild neurosensory hearing impairment 		35 0 32 0.36 0 0
CUI: C2931498
Disease: Mental Retardation, X-Linked 1
Mental Retardation, X-Linked 1 		45 0 32 0.33 0 0
CUI: C1858036
Disease: Periorbital fullness
Periorbital fullness 		57 0 34 0.31 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum 		63 0 34 0.30 0 0
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure 		73 0 34 0.27 0 0
CUI: C0013132
Disease: Drooling
Drooling 		95 14 37 0.26 2 7.1E-02
CUI: C0034194
Disease: Pyloric Stenosis
Pyloric Stenosis 		121 0 38 0.23 0 0
CUI: C0239174
Disease: Late tooth eruption
Late tooth eruption 		139 0 41 0.22 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities 		112 10 35 0.22 1 4.0E-02
CUI: C0426429
Disease: Broad nasal tip
Broad nasal tip 		125 0 33 0.19 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 35 0.18 0 0
CUI: C0042024
Disease: Urinary Incontinence
Urinary Incontinence 		151 14 35 0.17 1 3.4E-02
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion 		211 0 43 0.17 0 0
CUI: C0302511
Disease: Small for gestational age fetus
Small for gestational age fetus 		156 0 35 0.17 0 0
CUI: C0235991
Disease: Small for gestational age (disorder)
Small for gestational age (disorder) 		181 34 36 0.16 2 4.2E-02
CUI: C3501611
Disease: Mental Retardation, X-Linked Nonsyndromic
Mental Retardation, X-Linked Nonsyndromic 		16 0 13 0.15 0 0
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked 		141 0 29 0.15 0 0
CUI: C1865014
Disease: Long philtrum
Long philtrum 		282 16 47 0.15 1 3.2E-02
CUI: C0015469
Disease: Facial paralysis
Facial paralysis 		182 0 34 0.15 0 0
CUI: C1853242
Disease: Midface retrusion
Midface retrusion 		228 0 39 0.14 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		261 0 43 0.14 0 0