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CTD Diseases (CD): Jervell-Lange Nielsen Syndrome

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Root: CD Hierarchy (CTD diseases from Comparative Toxicogenomics Database)

Shortest distance to current term
(+ for parents, - for children)
CD term [CD ID] <#Children> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + + 6:   Diseases [MESH:C] <25>
+ + + + + 5:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + + 4:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + + 4:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + + 4:   Cardiovascular Diseases [MESH:D002318] <5>(37|36) (38|13|9)
+ + + 3:   Pathologic Processes [MESH:D010335] <65>(45|54) (50|27|12)
+ + + 3:   Heart Diseases [MESH:D006331] <31>(16|16) (19|5|4)
+ + + 3:   Cardiovascular Abnormalities [MESH:D018376] <6>(2|4) (3|1|2)
+ + 2:   Cardiac Conduction System Disease [MESH:D000075224] <12>(1|1) (1|0|0)
+ + 2:   Arrhythmias, Cardiac [MESH:D001145] <27>(2|2) (2|0|0)
+ + 2:   Heart Defects, Congenital [MESH:D006330] <142>(2|4) (3|0|2)
+ 1:   Long QT Syndrome [MESH:D008133] <20>(1|1) (1|0|0)
0:   Jervell-Lange Nielsen Syndrome [MESH:D029593] <1>(0|0) (0|0|0)
- 1:   Jervell And Lange-Nielsen Syndrome 2 [MESH:C567343](0|0) (0|0|0)