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CTD Diseases (CD): 17,20-Lyase Deficiency, Isolated

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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)
+ + + + + + + 7:   Diseases [MESH:C] <25>
+ + + + + + 6:   Female Urogenital Diseases and Pregnancy Complications [MESH:D005261] <2>(47|58) (50|27|10)
+ + + + + 5:   Male Urogenital Diseases [MESH:D052801] <7>(38|49) (38|20|8)
+ + + + + 5:   Nutritional and Metabolic Diseases [MESH:D009750] <2>(51|55) (57|23|4)
+ + + + + 5:   Female Urogenital Diseases [MESH:D052776] <6>(41|50) (42|22|9)
+ + + + + 5:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + + 4:   Metabolic Diseases [MESH:D008659] <23>(49|55) (54|22|4)
+ + + + 4:   Gonadal Disorders [MESH:D006058] <6>(5|4) (5|1|0)
+ + + + 4:   Urogenital Abnormalities [MESH:D014564] <52>(3|3) (3|1|0)
+ + + 3:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + 3:   Endocrine System Diseases [MESH:D004700] <18>(19|28) (22|15|10)
+ + + 3:   Metabolism, Inborn Errors [MESH:D008661] <143>(26|22) (28|7|1)
+ + + 3:   Disorders of Sex Development [MESH:D012734] <8>(2|2) (2|0|0)
+ + 2:   Genetic Diseases, Inborn [MESH:D030342] <75>(79|83) (83|37|18)
+ + 2:   Adrenogenital Syndrome [MESH:D047808] <2>(1|1) (1|0|0)
+ + 2:   Adrenal Gland Diseases [MESH:D000307] <8>(4|3) (4|0|0)
+ + 2:   Steroid Metabolism, Inborn Errors [MESH:D043202] <18>(2|2) (2|0|0)
+ 1:   Adrenal Hyperplasia, Congenital [MESH:D000312] <9>(1|1) (1|0|0)
0:   17,20-Lyase Deficiency, Isolated [MESH:C567076](0|0) (0|0|0)