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: C0238286
Disease: Mucolipidosis Type IV
Mucolipidosis Type IV 		22 0 3 7.7E-02 0 0
CUI: C3544321
Disease: Treatment-resistant schizophrenia
Treatment-resistant schizophrenia 		23 0 3 7.5E-02 0 0
CUI: C0011251
Disease: Delusional disorder
Delusional disorder 		9 0 2 7.4E-02 0 0
CUI: C0238378
Disease: Desquamative interstitial pneumonia
Desquamative interstitial pneumonia 		9 0 2 7.4E-02 0 0
CUI: C0887850
Disease: Polycystic Kidney, Type 1 Autosomal Dominant Disease
Polycystic Kidney, Type 1 Autosomal Dominant Disease 		10 0 2 7.1E-02 0 0
CUI: C0948444
Disease: Mitochondrial DNA mutation
Mitochondrial DNA mutation 		25 0 3 7.1E-02 0 0
CUI: C0030662
Disease: Gambling, Pathological
Gambling, Pathological 		26 9 3 7.0E-02 1 0.11
CUI: C2317473
Disease: Chronic kidney disease stage 4
Chronic kidney disease stage 4 		11 0 2 6.9E-02 0 0
CUI: C0036939
Disease: Shared Paranoid Disorder
Shared Paranoid Disorder 		27 0 3 6.8E-02 0 0
CUI: C0012734
Disease: Disruptive Behavior Disorder
Disruptive Behavior Disorder 		13 0 2 6.5E-02 0 0
CUI: C0859886
Disease: Inherited hearing loss
Inherited hearing loss 		13 0 2 6.5E-02 0 0
CUI: C1835686
Disease: Recurrent bacterial skin infections
Recurrent bacterial skin infections 		13 0 2 6.5E-02 0 0
CUI: C0233762
Disease: Hallucinations, Auditory
Hallucinations, Auditory 		14 0 2 6.2E-02 0 0
CUI: C0410173
Disease: Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)
Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder) 		14 0 2 6.2E-02 0 0
CUI: C0020225
Disease: Hydranencephaly
Hydranencephaly 		15 0 2 6.1E-02 0 0
CUI: C1969913
Disease: Generalized hyperkeratosis
Generalized hyperkeratosis 		16 0 2 5.9E-02 0 0
CUI: C0522174
Disease: Delinquent behavior
Delinquent behavior 		17 0 2 5.7E-02 0 0
CUI: C0266427
Disease: Testicular regression syndrome
Testicular regression syndrome 		37 0 3 5.6E-02 0 0
CUI: C1833225
Disease: Dystrophic toenail
Dystrophic toenail 		18 0 2 5.6E-02 0 0
CUI: C3541517
Disease: ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT 		18 0 2 5.6E-02 0 0
CUI: C3888065
Disease: ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT 		18 0 2 5.6E-02 0 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		38 0 3 5.5E-02 0 0
CUI: C0809983
Disease: Schizophrenia and related disorders
Schizophrenia and related disorders 		20 0 2 5.3E-02 0 0
CUI: C0855228
Disease: Eating disorder symptom
Eating disorder symptom 		20 0 2 5.3E-02 0 0
CUI: C0865424
Disease: Adult attention deficit hyperactivity disorder
Adult attention deficit hyperactivity disorder 		20 0 2 5.3E-02 0 0