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: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		103 0 1 8.8E-03 0 0
CUI: C4025596
Disease: Abnormality of connective tissue
Abnormality of connective tissue 		3 0 1 7.1E-02 0 0
CUI: C1866129
Disease: Abnormality of the cerebellum
Abnormality of the cerebellum 		8 11 1 5.3E-02 1 4.0E-02
CUI: C0744356
Disease: Abnormality of the genital system
Abnormality of the genital system 		5 4 1 6.2E-02 1 5.6E-02
CUI: C4021742
Disease: Abnormality of the humerus
Abnormality of the humerus 		1 0 1 8.3E-02 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		11 0 1 4.5E-02 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		46 0 1 1.8E-02 0 0
CUI: C4017118
Disease: ADULT POLYGLUCOSAN BODY NEUROPATHY
ADULT POLYGLUCOSAN BODY NEUROPATHY 		1 0 1 8.3E-02 0 0
CUI: C0002962
Disease: Angina Pectoris
Angina Pectoris 		2 0 1 7.7E-02 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		9 0 1 5.0E-02 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		16 25 10 0.56 13 0.48
CUI: C0220666
Disease: ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA 		1 3 1 8.3E-02 1 5.9E-02
CUI: C4310692
Disease: ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH
ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH 		1 11 1 8.3E-02 1 4.0E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		2 0 1 7.7E-02 0 0
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10 		1 0 1 8.3E-02 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		37 0 1 2.1E-02 0 0
CUI: C4016652
Disease: ATRIAL STANDSTILL 1, DIGENIC
ATRIAL STANDSTILL 1, DIGENIC 		1 0 1 8.3E-02 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		54 0 1 1.5E-02 0 0
CUI: C3711387
Disease: Autosomal Recessive Primary Microcephaly
Autosomal Recessive Primary Microcephaly 		6 0 1 5.9E-02 0 0
CUI: C1865186
Disease: Bell-shaped thorax
Bell-shaped thorax 		5 7 1 6.2E-02 1 4.8E-02
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		37 0 1 2.1E-02 0 0
CUI: C1862112
Disease: BRACHYDACTYLY, TYPE B1
BRACHYDACTYLY, TYPE B1 		1 0 1 8.3E-02 0 0
CUI: C3808046
Disease: Breathing dysregulation
Breathing dysregulation 		6 0 1 5.9E-02 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		3 0 1 7.1E-02 0 0
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		1 0 1 8.3E-02 0 0