Source: CLINVAR ×
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: C0001807
Disease: Aggressive behavior
Aggressive behavior 		13 0 1 1.1E-02 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		17 0 1 1.1E-02 0 0
CUI: C0003467
Disease: Anxiety
Anxiety 		13 20 1 1.1E-02 1 4.2E-03
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		54 0 1 7.6E-03 0 0
CUI: C0006325
Disease: Bruxism
Bruxism 		4 0 1 1.2E-02 0 0
CUI: C0008525
Disease: Choroideremia
Choroideremia 		1 0 1 1.3E-02 0 0
CUI: C0008732
Disease: Chylous Ascites
Chylous Ascites 		1 0 1 1.3E-02 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		36 0 1 8.8E-03 0 0
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital 		3 2 1 1.3E-02 1 4.6E-03
CUI: C0009806
Disease: Constipation
Constipation 		40 0 1 8.5E-03 0 0
CUI: C0011334
Disease: Dental caries
Dental caries 		7 0 1 1.2E-02 0 0
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		29 0 1 9.4E-03 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism 		9 13 1 1.2E-02 2 8.7E-03
CUI: C0013362
Disease: Dysarthria
Dysarthria 		34 0 1 9.0E-03 0 0
CUI: C0013363
Disease: Dysautonomia
Dysautonomia 		9 9 1 1.2E-02 1 4.4E-03
CUI: C0013528
Disease: Echolalia
Echolalia 		2 0 1 1.3E-02 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		6 0 1 1.2E-02 0 0
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		8 0 1 1.2E-02 0 0
CUI: C0018780
Disease: Hearing Loss, High-Frequency
Hearing Loss, High-Frequency 		1 1 1 1.3E-02 1 4.6E-03
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		21 30 1 1.0E-02 1 4.0E-03
CUI: C0019214
Disease: Hepatosplenomegaly
Hepatosplenomegaly 		15 0 1 1.1E-02 0 0
CUI: C0019572
Disease: Hirsutism
Hirsutism 		12 0 1 1.1E-02 0 0
CUI: C0020505
Disease: Hyperphagia
Hyperphagia 		3 0 1 1.3E-02 0 0
CUI: C0020619
Disease: Hypogonadism
Hypogonadism 		6 0 1 1.2E-02 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		14 0 1 1.1E-02 0 0