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CTD Diseases (CD): TUMOR PREDISPOSITION 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)
+ + + + + 5:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + + 4:   Pathologic Processes [MESH:D010335] <65>(45|54) (50|27|12)
+ + + 3:   Disease Attributes [MESH:D020969] <20>(3|6) (3|6|4)
+ + 2:   Diseases [MESH:C] <25>
+ + 2:   Disease Susceptibility [MESH:D004198] <3>(1|2) (1|1|0)
+ 1:   Neoplasms [MESH:D009369] <18>(68|96) (74|65|31)
+ 1:   Genetic Predisposition to Disease [MESH:D020022] <3>(0|0) (0|0|0)
0:   TUMOR PREDISPOSITION SYNDROME [OMIM:614327](0|0) (0|0|0)