Source: INFERRED ×
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: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome 		18 0 3 0.11 0 0
CUI: C0332878
Disease: Congenital contracture
Congenital contracture 		18 0 3 0.11 0 0
CUI: C4021262
Disease: Absent palmar crease
Absent palmar crease 		9 0 2 0.11 0 0
CUI: C4021774
Disease: Camptodactyly of toe
Camptodactyly of toe 		9 0 2 0.11 0 0
CUI: C0749379
Disease: Thoracolumbar scoliosis
Thoracolumbar scoliosis 		20 0 3 0.10 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: C0239272
Disease: Elbow stiff
Elbow stiff 		1 0 1 8.3E-02 0 0
CUI: C0264913
Disease: Left posterior fascicular block
Left posterior fascicular block 		1 0 1 8.3E-02 0 0
CUI: C0265227
Disease: Schinzel-Giedion syndrome
Schinzel-Giedion syndrome 		1 8 1 8.3E-02 1 4.5E-02
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		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: 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: C1849307
Disease: Increased density of long bones
Increased density of long bones 		1 0 1 8.3E-02 0 0
CUI: C1849309
Disease: Wide distal femoral metaphysis
Wide distal femoral metaphysis 		1 0 1 8.3E-02 0 0
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
CUI: C1856301
Disease: GSD IV, Classic Hepatic
GSD IV, Classic Hepatic 		1 0 1 8.3E-02 0 0
CUI: C1856304
Disease: GSD IV, Neuromuscular Form, Congenital
GSD IV, Neuromuscular Form, Congenital 		1 0 1 8.3E-02 0 0
CUI: C1856305
Disease: GSD IV, Neuromuscular Form, Childhood
GSD IV, Neuromuscular Form, Childhood 		1 0 1 8.3E-02 0 0
CUI: C1859062
Disease: LONG QT SYNDROME 3
LONG QT SYNDROME 3 		1 0 1 8.3E-02 0 0
CUI: C1861983
Disease: Heart Block, Nonprogressive
Heart Block, Nonprogressive 		1 0 1 8.3E-02 0 0