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: C0003886
Disease: Arthrogryposis
Arthrogryposis 		16 25 10 0.56 13 0.48
CUI: C0332878
Disease: Congenital contracture
Congenital contracture 		2 0 2 0.17 0 0
CUI: C0240912
Disease: Vertical Talus
Vertical Talus 		6 6 2 0.12 1 5.0E-02
CUI: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome 		8 0 2 0.11 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		8 7 2 0.11 1 4.8E-02
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal 		9 0 2 0.11 0 0
CUI: C0749379
Disease: Thoracolumbar scoliosis
Thoracolumbar scoliosis 		12 0 2 9.1E-02 0 0
CUI: C0024591
Disease: Malignant hyperpyrexia due to anesthesia
Malignant hyperpyrexia due to anesthesia 		1 0 1 8.3E-02 0 0
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome 		1 0 1 8.3E-02 0 0
CUI: C0038018
Disease: Spondylolysis
Spondylolysis 		1 0 1 8.3E-02 0 0
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: C0265227
Disease: Schinzel-Giedion syndrome
Schinzel-Giedion syndrome 		1 8 1 8.3E-02 1 4.5E-02
CUI: C0344490
Disease: Sacral agenesis
Sacral agenesis 		1 0 1 8.3E-02 0 0
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		1 0 1 8.3E-02 0 0
CUI: C0575803
Disease: Radial deviation of hand
Radial deviation of hand 		1 0 1 8.3E-02 0 0
CUI: C0751951
Disease: Central Core Myopathy (disorder)
Central Core Myopathy (disorder) 		1 0 1 8.3E-02 0 0
CUI: C0796033
Disease: MARDEN-WALKER SYNDROME
MARDEN-WALKER SYNDROME 		1 0 1 8.3E-02 0 0
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E 		1 0 1 8.3E-02 0 0
CUI: C1837501
Disease: Microcephaly, Primary Autosomal Recessive, 5
Microcephaly, Primary Autosomal Recessive, 5 		1 0 1 8.3E-02 0 0
CUI: C1837761
Disease: Narrow nasal ridge
Narrow nasal ridge 		1 0 1 8.3E-02 0 0
CUI: C1837845
Disease: SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE 		1 0 1 8.3E-02 0 0
CUI: C1838527
Disease: LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding) 		1 0 1 8.3E-02 0 0
CUI: C1849295
Disease: Hypoplastic labia minora
Hypoplastic labia minora 		1 1 1 8.3E-02 1 6.7E-02
CUI: C1849334
Disease: Robinow syndrome, autosomal recessive
Robinow syndrome, autosomal recessive 		1 0 1 8.3E-02 0 0
CUI: C1849722
Disease: Polyglucosan Body Disease, Adult Form
Polyglucosan Body Disease, Adult Form 		1 0 1 8.3E-02 0 0