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CTD Diseases (CD): AREDYLD 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:   Nutritional and Metabolic Diseases [MESH:D009750] <2>(51|55) (57|23|4)
+ + + + + 5:   Metabolic Diseases [MESH:D008659] <23>(49|55) (54|22|4)
+ + + + + 5:   Diseases [MESH:C] <25>
+ + + + 4:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + + 4:   Glucose Metabolism Disorders [MESH:D044882] <8>(7|11) (9|5|2)
+ + + + 4:   Endocrine System Diseases [MESH:D004700] <18>(19|28) (22|15|10)
+ + + + 4:   Skin and Connective Tissue Diseases [MESH:D017437] <2>(38|43) (41|28|20)
+ + + 3:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + 3:   Skin Diseases [MESH:D012871] <71>(31|34) (31|22|11)
+ + + 3:   Genetic Diseases, Inborn [MESH:D030342] <75>(79|83) (83|37|18)
+ + + 3:   Diabetes Mellitus [MESH:D003920] <44>(3|7) (5|4|2)
+ + + 3:   Stomatognathic Diseases [MESH:D009057] <7>(9|14) (12|8|4)
+ + 2:   Abnormalities, Multiple [MESH:D000015] <389>(12|10) (12|4|3)
+ + 2:   Skin Abnormalities [MESH:D012868] <63>(7|8) (7|5|1)
+ + 2:   Stomatognathic System Abnormalities [MESH:D018640] <5>(1|2) (3|3|1)
+ + 2:   Skin Diseases, Genetic [MESH:D012873] <76>(8|10) (8|4|1)
+ + 2:   Tooth Diseases [MESH:D014076] <26>(0|0) (1|2|0)
+ + 2:   Diabetes Mellitus, Type 2 [MESH:D003924] <19>(0|3) (1|1|0)
+ 1:   Diabetes Mellitus, Lipoatrophic [MESH:D003923] <1>(0|0) (0|0|0)
+ 1:   Ectodermal Dysplasia [MESH:D004476] <97>(1|2) (1|0|0)
+ 1:   Tooth Abnormalities [MESH:D014071] <53>(0|0) (1|2|0)
0:   AREDYLD Syndrome [MESH:C537427](0|0) (0|0|0)