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: C0000737
Disease: Abdominal Pain
Abdominal Pain 		9 0 1 1.3E-02 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		8 0 1 1.4E-02 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		17 0 1 1.2E-02 0 0
CUI: C0002940
Disease: Aneurysm
Aneurysm 		12 0 1 1.3E-02 0 0
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation 		3 0 1 1.4E-02 0 0
CUI: C0004114
Disease: Astrocytoma
Astrocytoma 		5 0 1 1.4E-02 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		37 0 1 9.7E-03 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		44 0 1 9.1E-03 0 0
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis 		4 0 1 1.4E-02 0 0
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		7 0 1 1.4E-02 0 0
CUI: C0011813
Disease: Dextrocardia
Dextrocardia 		6 0 1 1.4E-02 0 0
CUI: C0013132
Disease: Drooling
Drooling 		14 0 1 1.3E-02 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism 		9 0 1 1.3E-02 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot 		30 0 1 1.0E-02 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma 		6 0 1 1.4E-02 0 0
CUI: C0017639
Disease: Gliosis
Gliosis 		4 0 1 1.4E-02 0 0
CUI: C0018022
Disease: Endemic goiter
Endemic goiter 		2 0 1 1.5E-02 0 0
CUI: C0018672
Disease: Head Banging
Head Banging 		3 0 1 1.4E-02 0 0
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		39 0 1 9.5E-03 0 0
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal 		13 0 2 2.6E-02 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		22 0 1 1.1E-02 0 0
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism 		4 0 1 1.4E-02 0 0
CUI: C0020555
Disease: Hypertrichosis
Hypertrichosis 		14 0 1 1.3E-02 0 0
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		25 0 2 2.2E-02 0 0
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes 		9 0 2 2.7E-02 0 0