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CTD Diseases (CD): Long QT 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)
+ + + + 4:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + + 4:   Diseases [MESH:C] <25>
+ + + 3:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + 3:   Cardiovascular Diseases [MESH:D002318] <5>(37|36) (38|13|9)
+ + + 3:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + 2:   Cardiovascular Abnormalities [MESH:D018376] <6>(2|4) (3|1|2)
+ + 2:   Pathologic Processes [MESH:D010335] <65>(45|54) (50|27|12)
+ + 2:   Heart Diseases [MESH:D006331] <31>(16|16) (19|5|4)
+ 1:   Cardiac Conduction System Disease [MESH:D000075224] <12>(1|1) (1|0|0)
+ 1:   Arrhythmias, Cardiac [MESH:D001145] <27>(2|2) (2|0|0)
+ 1:   Heart Defects, Congenital [MESH:D006330] <142>(2|4) (3|0|2)
0:   Long QT Syndrome [MESH:D008133] <20>(1|1) (1|0|0)
- 1:   Jervell-Lange Nielsen Syndrome [MESH:D029593] <1>(0|0) (0|0|0)
- 1:   Romano-Ward Syndrome [MESH:D029597] <1>(0|0) (0|0|0)
- 1:   Andersen Syndrome [MESH:D050030](0|0) (0|0|0)
- 1:   LONG QT SYNDROME 13 [OMIM:613485](0|0) (0|0|0)
- 1:   LONG QT SYNDROME 14 [OMIM:616247](0|0) (0|0|0)
- 1:   LONG QT SYNDROME 15 [OMIM:616249](0|0) (0|0|0)
- 1:   Long QT syndrome type 3 [MESH:C537034](0|0) (0|0|0)
- 1:   Long Qt Syndrome 10 [MESH:C567514](0|0) (0|0|0)
- 1:   Long Qt Syndrome 11 [MESH:C567513](0|0) (0|0|0)
- 1:   Long Qt Syndrome 12 [MESH:C567842](0|0) (0|0|0)
- 1:   Long Qt Syndrome 2 [MESH:C563614](0|0) (0|0|0)
- 1:   Long Qt Syndrome 2-3 [MESH:C565841](0|0) (0|0|0)
- 1:   Long Qt Syndrome 2-5 [MESH:C566765](0|0) (0|0|0)
- 1:   Long Qt Syndrome 3 [MESH:C565840](0|0) (0|0|0)
- 1:   Long Qt Syndrome 3-6 [MESH:C566334](0|0) (0|0|0)
- 1:   Long Qt Syndrome 4 [MESH:C563428](0|0) (0|0|0)
- 1:   Long Qt Syndrome 5 [MESH:C566766](0|0) (0|0|0)
- 1:   Long Qt Syndrome 6 [MESH:C566333](0|0) (0|0|0)
- 1:   Long Qt Syndrome 9 [MESH:C567515](0|0) (0|0|0)
- 1:   Timothy syndrome [MESH:C536962](0|0) (0|0|0)

Superfamily

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Superfamily

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SCOP term FDR (all) Annotation (direct or inherited)
Voltage-gated potassium channels0.00001188Direct

LINKTO: Domain2BO Download and Domain2BO Algorithm

Family

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Family

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SCOP term FDR (all) Annotation (direct or inherited)
Voltage-gated potassium channels0.0001814Direct

LINKTO: Domain2BO Download and Domain2BO Algorithm

Supra-domain (Single|Duplex|Triple)

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Supra-domain (Single)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Voltage-gated potassium channels0.000005911Direct

LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm

Distribution on sTOL

Plot distribution on species Tree Of Life (sTOL) for Superfamily and/or Family domains annotated by this CD term
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Plot distribution on species Tree Of Life (sTOL) for single supra-domains annotated by this CD term
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