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: C0871215
Disease: Reading Disabilities
Reading Disabilities 		28 3 9 0.17 1 2.9E-02
CUI: C0037789
Disease: Specific reading disorder
Specific reading disorder 		6 0 5 0.15 0 0
CUI: C0476254
Disease: Dyslexia
Dyslexia 		118 30 19 0.14 7 0.13
CUI: C0038506
Disease: Stuttering
Stuttering 		34 0 7 0.12 0 0
CUI: C0457334
Disease: Acute monoblastic leukemia
Acute monoblastic leukemia 		37 0 7 0.11 0 0
CUI: C3711376
Disease: Isodicentric Chromosome 15 Syndrome
Isodicentric Chromosome 15 Syndrome 		39 0 7 0.11 0 0
CUI: C0010418
Disease: Cryptosporidiosis
Cryptosporidiosis 		40 0 7 0.11 0 0
CUI: C0751529
Disease: Stuttering, Developmental
Stuttering, Developmental 		13 0 4 9.5E-02 0 0
CUI: C0751528
Disease: Stuttering, Childhood
Stuttering, Childhood 		3 0 3 9.1E-02 0 0
CUI: C2004345
Disease: phonological developmental disorder
phonological developmental disorder 		5 0 3 8.6E-02 0 0
CUI: C4019167
Disease: Speech Sound Disorders
Speech Sound Disorders 		11 0 3 7.3E-02 0 0
CUI: C0012734
Disease: Disruptive Behavior Disorder
Disruptive Behavior Disorder 		13 0 3 7.0E-02 0 0
CUI: C0023014
Disease: Language Development Disorders
Language Development Disorders 		18 0 3 6.2E-02 0 0
CUI: C2874392
Disease: Alcohol dependence with withdrawal, unspecified
Alcohol dependence with withdrawal, unspecified 		2 0 2 6.1E-02 0 0
CUI: C2673377
Disease: MUCOLIPIDOSIS II ALPHA/BETA (disorder)
MUCOLIPIDOSIS II ALPHA/BETA (disorder) 		3 0 2 5.9E-02 0 0
CUI: C0023015
Disease: Language Disorders
Language Disorders 		94 0 7 5.8E-02 0 0
CUI: C0349391
Disease: Apraxia, Verbal
Apraxia, Verbal 		4 0 2 5.7E-02 0 0
CUI: C0268318
Disease: Cholestasis of pregnancy
Cholestasis of pregnancy 		100 0 7 5.6E-02 0 0
CUI: C0154209
Disease: Hyperestrogenism
Hyperestrogenism 		6 0 2 5.4E-02 0 0
CUI: C0236818
Disease: Selective Mutism
Selective Mutism 		6 0 2 5.4E-02 0 0
CUI: C1456326
Disease: Selective mutism specific to childhood and adolescence
Selective mutism specific to childhood and adolescence 		6 0 2 5.4E-02 0 0
CUI: C3274639
Disease: Neonatal Opiate Withdrawal Syndrome
Neonatal Opiate Withdrawal Syndrome 		6 0 2 5.4E-02 0 0
CUI: C0029121
Disease: Oppositional Defiant Disorder
Oppositional Defiant Disorder 		27 0 3 5.3E-02 0 0
CUI: C0033788
Disease: Pseudo-Hurler Polydystrophy
Pseudo-Hurler Polydystrophy 		7 0 2 5.3E-02 0 0
CUI: C0008043
Disease: Chiari-Frommel Syndrome
Chiari-Frommel Syndrome 		9 0 2 5.0E-02 0 0