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: C0233726
Disease: Aprosodia
Aprosodia 		3 0 3 1.00 0 0
CUI: C0751512
Disease: Dysglossia
Dysglossia 		3 0 3 1.00 0 0
CUI: C0751513
Disease: Rhinolalia
Rhinolalia 		3 0 3 1.00 0 0
CUI: C3495145
Disease: Dyslalia
Dyslalia 		4 0 3 0.75 0 0
CUI: C0009090
Disease: Cluttering
Cluttering 		8 0 3 0.38 0 0
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction 		1 0 1 0.33 0 0
CUI: C4016662
Disease: ATAXIA, FRIEDREICH-LIKE, WITH ISOLATED VITAMIN E DEFICIENCY
ATAXIA, FRIEDREICH-LIKE, WITH ISOLATED VITAMIN E DEFICIENCY 		1 0 1 0.33 0 0
CUI: C4016663
Disease: ATAXIA AND RETINITIS PIGMENTOSA WITH ISOLATED VITAMIN E DEFICIENCY
ATAXIA AND RETINITIS PIGMENTOSA WITH ISOLATED VITAMIN E DEFICIENCY 		1 0 1 0.33 0 0
CUI: C4225310
Disease: MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE 		1 0 1 0.33 0 0
CUI: C4749281
Disease: Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation 		1 0 1 0.33 0 0
CUI: C0027438
Disease: Nasopharyngeal Diseases
Nasopharyngeal Diseases 		2 0 1 0.25 0 0
CUI: C0282512
Disease: Landau-Kleffner Syndrome
Landau-Kleffner Syndrome 		2 0 1 0.25 0 0
CUI: C0752255
Disease: Impairment, Light Touch Sensation
Impairment, Light Touch Sensation 		2 0 1 0.25 0 0
CUI: C0752256
Disease: Pain Sensation Diminished
Pain Sensation Diminished 		2 0 1 0.25 0 0
CUI: C0752257
Disease: Pinprick Sensation Diminished
Pinprick Sensation Diminished 		2 0 1 0.25 0 0
CUI: C0752258
Disease: Position Sense Disorders
Position Sense Disorders 		2 0 1 0.25 0 0
CUI: C0752260
Disease: Proprioceptive Disorders
Proprioceptive Disorders 		2 0 1 0.25 0 0
CUI: C0752261
Disease: Thermal Sensation Disorders
Thermal Sensation Disorders 		2 0 1 0.25 0 0
CUI: C0752262
Disease: Somatosensory Disorders
Somatosensory Disorders 		2 0 1 0.25 0 0
CUI: C1112263
Disease: Atypical benign partial epilepsy
Atypical benign partial epilepsy 		2 0 1 0.25 0 0
CUI: C3806402
Disease: EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION 		2 0 1 0.25 0 0
CUI: C0155536
Disease: Paracousis
Paracousis 		3 0 1 0.20 0 0
CUI: C0260662
Disease: Hearing problem
Hearing problem 		3 0 1 0.20 0 0
CUI: C0877848
Disease: Distorted hearing
Distorted hearing 		3 0 1 0.20 0 0
CUI: C1510450
Disease: Dysacusis
Dysacusis 		3 0 1 0.20 0 0