Source: CURATED ×
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: C0023012
Disease: Language Delay
Language Delay 		11 0 11 1.00 0 0
CUI: C0023014
Disease: Language Development Disorders
Language Development Disorders 		11 0 11 1.00 0 0
CUI: C0454655
Disease: Semantic-Pragmatic Disorder
Semantic-Pragmatic Disorder 		11 0 11 1.00 0 0
CUI: C0751257
Disease: Auditory Processing Disorder, Central
Auditory Processing Disorder, Central 		11 0 11 1.00 0 0
CUI: C0003635
Disease: Apraxias
Apraxias 		2 0 2 0.18 0 0
CUI: C0234526
Disease: Ideational Apraxia
Ideational Apraxia 		2 0 2 0.18 0 0
CUI: C0234527
Disease: Apraxia, Motor
Apraxia, Motor 		2 0 2 0.18 0 0
CUI: C0234529
Disease: Dressing Apraxia
Dressing Apraxia 		2 0 2 0.18 0 0
CUI: C0349391
Disease: Apraxia, Verbal
Apraxia, Verbal 		2 0 2 0.18 0 0
CUI: C0422892
Disease: Apraxia, Gestural
Apraxia, Gestural 		2 0 2 0.18 0 0
CUI: C0454608
Disease: Apraxia, Oral
Apraxia, Oral 		2 0 2 0.18 0 0
CUI: C0750927
Disease: Apraxia, Developmental Verbal
Apraxia, Developmental Verbal 		2 0 2 0.18 0 0
CUI: C0750928
Disease: Apraxia, Facial-Oral
Apraxia, Facial-Oral 		2 0 2 0.18 0 0
CUI: C3495144
Disease: Apraxia, Articulatory
Apraxia, Articulatory 		2 0 2 0.18 0 0
CUI: C0264611
Disease: Apraxia of Phonation
Apraxia of Phonation 		3 0 2 0.17 0 0
CUI: C1970431
Disease: PITT-HOPKINS SYNDROME
PITT-HOPKINS SYNDROME 		3 0 2 0.17 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		17 0 3 0.12 0 0
CUI: C0003081
Disease: Anisometropia
Anisometropia 		1 0 1 9.1E-02 0 0
CUI: C0023801
Disease: Lipomatosis
Lipomatosis 		1 0 1 9.1E-02 0 0
CUI: C0034139
Disease: Purine-Pyrimidine Metabolism, Inborn Errors
Purine-Pyrimidine Metabolism, Inborn Errors 		1 0 1 9.1E-02 0 0
CUI: C0038131
Disease: Stammering
Stammering 		1 0 1 9.1E-02 0 0
CUI: C0038506
Disease: Stuttering
Stuttering 		1 0 1 9.1E-02 0 0
CUI: C0282512
Disease: Landau-Kleffner Syndrome
Landau-Kleffner Syndrome 		1 0 1 9.1E-02 0 0
CUI: C0454542
Disease: Stuttering, Acquired
Stuttering, Acquired 		1 0 1 9.1E-02 0 0
CUI: C0454651
Disease: Specific language impairment
Specific language impairment 		1 0 1 9.1E-02 0 0