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CTD Diseases (CD): Roifman-Chitayat 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:   Diseases [MESH:C] <25>
+ + + + 4:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + 3:   Nervous System Diseases [MESH:D009422] <27>(86|87) (91|33|8)
+ + + 3:   Mental Disorders [MESH:D001523] <27>(22|26) (25|8|3)
+ + + 3:   Immune System Diseases [MESH:D007154] <18>(36|47) (41|22|8)
+ + + 3:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + 3:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + + 3:   Pathologic Processes [MESH:D010335] <65>(45|54) (50|27|12)
+ + 2:   Eye Diseases [MESH:D005128] <31>(8|6) (9|6|7)
+ + 2:   Immunologic Deficiency Syndromes [MESH:D007153] <95>(15|15) (15|5|1)
+ + 2:   Neurodevelopmental Disorders [MESH:D065886] <17>(9|11) (12|5|2)
+ + 2:   Genetic Diseases, Inborn [MESH:D030342] <75>(79|83) (83|37|18)
+ + 2:   Cranial Nerve Diseases [MESH:D003389] <17>(1|1) (1|0|0)
+ + 2:   Bone Diseases [MESH:D001847] <34>(10|9) (12|6|4)
+ + 2:   Disease Attributes [MESH:D020969] <20>(3|6) (3|6|4)
+ 1:   Bone Diseases, Developmental [MESH:D001848] <89>(2|4) (2|4|3)
+ 1:   Optic Nerve Diseases [MESH:D009901] <14>(0|0) (0|0|0)
+ 1:   Developmental Disabilities [MESH:D002658] <57>(0|0) (0|0|0)
+ 1:   Facies [MESH:D019066] <151>(0|0) (0|0|0)
+ 1:   Primary Immunodeficiency Diseases [MESH:D000081207] <40>(8|8) (8|2|0)
0:   Roifman-Chitayat Syndrome [MESH:C567641](0|0) (0|0|0)