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: C0038131
Disease: Stammering
Stammering 		1 0 1 0.33 0 0
CUI: C0038506
Disease: Stuttering
Stuttering 		1 0 1 0.33 0 0
CUI: C0454542
Disease: Stuttering, Acquired
Stuttering, Acquired 		1 0 1 0.33 0 0
CUI: C0751527
Disease: Stuttering, Adult
Stuttering, Adult 		1 0 1 0.33 0 0
CUI: C0751528
Disease: Stuttering, Childhood
Stuttering, Childhood 		1 0 1 0.33 0 0
CUI: C0751529
Disease: Stuttering, Developmental
Stuttering, Developmental 		1 0 1 0.33 0 0
CUI: C2750246
Disease: Pitt-Hopkins-Like Syndrome 1
Pitt-Hopkins-Like Syndrome 1 		1 0 1 0.33 0 0
CUI: C2750451
Disease: CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3 		1 2 1 0.33 2 3.4E-02
CUI: C3280479
Disease: PITT-HOPKINS-LIKE SYNDROME 2
PITT-HOPKINS-LIKE SYNDROME 2 		1 0 1 0.33 0 0
CUI: C3808494
Disease: CHROMOSOME 2p16.3 DELETION SYNDROME
CHROMOSOME 2p16.3 DELETION SYNDROME 		1 0 1 0.33 0 0
CUI: C4552043
Disease: Cortical dysplasia with focal epilepsy syndrome
Cortical dysplasia with focal epilepsy syndrome 		1 0 1 0.33 0 0
CUI: C3489627
Disease: Stuttering, Familial Persistent 1
Stuttering, Familial Persistent 1 		2 0 1 0.25 0 0
CUI: C0023012
Disease: Language Delay
Language Delay 		11 0 2 0.17 0 0
CUI: C0023014
Disease: Language Development Disorders
Language Development Disorders 		11 0 2 0.17 0 0
CUI: C0241210
Disease: Speech Delay
Speech Delay 		11 0 2 0.17 0 0
CUI: C0454655
Disease: Semantic-Pragmatic Disorder
Semantic-Pragmatic Disorder 		11 0 2 0.17 0 0
CUI: C0751257
Disease: Auditory Processing Disorder, Central
Auditory Processing Disorder, Central 		11 0 2 0.17 0 0
CUI: C0016781
Disease: Fuchs Endothelial Dystrophy
Fuchs Endothelial Dystrophy 		5 0 1 0.14 0 0
CUI: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis 		8 0 1 1.0E-01 0 0
CUI: C1456784
Disease: Paranoia
Paranoia 		11 0 1 7.7E-02 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		17 0 1 5.3E-02 0 0
CUI: C3853041
Disease: Severe Congenital Microcephaly
Severe Congenital Microcephaly 		31 0 1 3.0E-02 0 0
CUI: C0751217
Disease: Hyperkinesia, Generalized
Hyperkinesia, Generalized 		32 0 1 2.9E-02 0 0
CUI: C3887506
Disease: Hyperkinesia
Hyperkinesia 		32 0 1 2.9E-02 0 0
CUI: C1956147
Disease: Microlissencephaly
Microlissencephaly 		33 0 1 2.9E-02 0 0