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CTD Diseases (CD): Intestinal Atresia

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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>
+ + + 3:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + 2:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + 2:   Digestive System Diseases [MESH:D004066] <9>(49|56) (59|39|21)
+ + 2:   Gastrointestinal Diseases [MESH:D005767] <13>(20|22) (23|12|7)
+ 1:   Intestinal Diseases [MESH:D007410] <30>(16|17) (19|7|3)
+ 1:   Digestive System Abnormalities [MESH:D004065] <18>(0|0) (0|0|0)
0:   Intestinal Atresia [MESH:D007409] <12>(0|0) (0|0|0)
- 1:   Atresia of small intestine [MESH:C538260](0|0) (0|0|0)
- 1:   Colonic Atresia [MESH:C562562](0|0) (0|0|0)
- 1:   Coronal synostosis, syndactyly and jejunal atresia [MESH:C536445](0|0) (0|0|0)
- 1:   Duodenojejunal atresia with volvulus, absent dorsal mesentery and absent superior mesenteric artery [MESH:C535722](0|0) (0|0|0)
- 1:   Familial duodenal atresia [MESH:C535720](0|0) (0|0|0)
- 1:   Intestinal Atresia, Multiple [MESH:C562441](0|0) (0|0|0)
- 1:   Jejunal Atresia with Microcephaly and Ocular Anomalies [MESH:C565460](0|0) (0|0|0)
- 1:   Jejunal atresia with renal adysplasia [MESH:C537567](0|0) (0|0|0)
- 1:   Martinez-Frias Syndrome [MESH:C563346](0|0) (0|0|0)
- 1:   Mitchell-Riley Syndrome [MESH:C567570](0|0) (0|0|0)
- 1:   Pfeiffer Rockelein syndrome [MESH:C537890](0|0) (0|0|0)
- 1:   Umbilical cord ulceration and intestinal atresia [MESH:C536938](0|0) (0|0|0)