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CTD Diseases (CD): Finnish lethal neonatal metabolic 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:   Male Urogenital Diseases [MESH:D052801] <7>(38|49) (38|20|8)
+ + + + + 5:   Female Urogenital Diseases [MESH:D052776] <6>(41|50) (42|22|9)
+ + + + 4:   Urologic Diseases [MESH:D014570] <9>(21|21) (21|8|3)
+ + + + 4:   Female Urogenital Diseases and Pregnancy Complications [MESH:D005261] <2>(47|58) (50|27|10)
+ + + + 4:   Diseases [MESH:C] <25>
+ + + + 4:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + + 4:   Digestive System Diseases [MESH:D004066] <9>(49|56) (59|39|21)
+ + + 3:   Pathologic Processes [MESH:D010335] <65>(45|54) (50|27|12)
+ + + 3:   Nutritional and Metabolic Diseases [MESH:D009750] <2>(51|55) (57|23|4)
+ + + 3:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + 3:   Biliary Tract Diseases [MESH:D001660] <6>(8|8) (10|5|3)
+ + + 3:   Acid-Base Imbalance [MESH:D000137] <5>(0|0) (0|0|0)
+ + + 3:   Iron Metabolism Disorders [MESH:D019189] <9>(0|0) (0|0|0)
+ + + 3:   Kidney Diseases [MESH:D007674] <65>(18|16) (18|5|3)
+ + + 3:   Pregnancy Complications [MESH:D011248] <33>(6|9) (9|5|1)
+ + 2:   Genetic Diseases, Inborn [MESH:D030342] <75>(79|83) (83|37|18)
+ + 2:   Acidosis [MESH:D000138] <7>(0|0) (0|0|0)
+ + 2:   Iron Overload [MESH:D019190] <3>(0|0) (0|0|0)
+ + 2:   Renal Tubular Transport, Inborn Errors [MESH:D015499] <27>(2|2) (2|0|0)
+ + 2:   Bile Duct Diseases [MESH:D001649] <6>(6|5) (7|3|1)
+ + 2:   Fetal Diseases [MESH:D005315] <14>(2|2) (2|1|0)
+ + 2:   Metabolic Diseases [MESH:D008659] <23>(49|55) (54|22|4)
+ + 2:   Growth Disorders [MESH:D006130] <185>(0|1) (0|0|0)
+ 1:   Mitochondrial Diseases [MESH:D028361] <64>(0|0) (0|0|0)
+ 1:   Fetal Growth Retardation [MESH:D005317] <25>(0|0) (0|0|0)
+ 1:   Hemosiderosis [MESH:D006486] <3>(0|0) (0|0|0)
+ 1:   Cholestasis [MESH:D002779] <14>(5|4) (6|1|0)
+ 1:   Acidosis, Lactic [MESH:D000140] <19>(0|0) (0|0|0)
+ 1:   Metabolism, Inborn Errors [MESH:D008661] <143>(26|22) (28|7|1)
+ 1:   Renal Aminoacidurias [MESH:D000608] <6>(0|0) (0|0|0)
0:   Finnish lethal neonatal metabolic syndrome [MESH:C537934](0|0) (0|0|0)