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 0.56 0 0
Moderate sensorineural hearing impairment
34 0 32 0.54 0 0
CUI: C1846151
Disease: Widened subarachnoid space
Widened subarachnoid space
35 0 32 0.53 0 0
Mild neurosensory hearing impairment
35 0 32 0.53 0 0
Shortening of all distal phalanges of the fingers
40 0 32 0.49 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum
59 0 32 0.38 0 0
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure
73 0 33 0.34 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 34 0.31 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
96 0 34 0.29 0 0
CUI: C0426429
Disease: Broad nasal tip
Broad nasal tip
125 8 40 0.28 1 9.1E-02
CUI: C0013132
Disease: Drooling
Drooling
94 0 33 0.28 0 0
CUI: C0034194
Disease: Pyloric Stenosis
Pyloric Stenosis
121 0 35 0.24 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities
111 0 33 0.24 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion
145 10 39 0.24 1 7.7E-02
CUI: C0239174
Disease: Late tooth eruption
Late tooth eruption
139 0 37 0.23 0 0
CUI: C0042024
Disease: Urinary Incontinence
Urinary Incontinence
140 0 33 0.20 0 0
CUI: C0015469
Disease: Facial paralysis
Facial paralysis
165 0 34 0.18 0 0
CUI: C0302511
Disease: Small for gestational age fetus
Small for gestational age fetus
156 0 32 0.18 0 0
Small for gestational age (disorder)
181 34 34 0.17 1 2.7E-02
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion
211 25 37 0.16 2 7.4E-02
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures
178 0 32 0.16 0 0
CUI: C1853242
Disease: Midface retrusion
Midface retrusion
228 0 38 0.15 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
223 0 37 0.15 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior
228 76 37 0.15 1 1.3E-02
CUI: C1848207
Disease: Poor speech
Poor speech
208 0 33 0.14 0 0