dcGO - A comprehensive domain-centric ontology resource for post-genomic research on functions, phenotypes, diseases and more   
  
  

CTD Diseases (CD): Methemoglobinemia

(show info)

Jump to [ Top · Hierarchy · Annotations ]

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)
+ + + 3:   Diseases [MESH:C] <25>
+ + 2:   Hemic and Lymphatic Diseases [MESH:D006425] <2>(28|35) (30|15|8)
+ 1:   Hematologic Diseases [MESH:D006402] <22>(16|16) (18|4|3)
0:   Methemoglobinemia [MESH:D008708] <6>(0|0) (0|0|0)
- 1:   Congenital Methemoglobinemia [MESH:C580280](0|0) (0|0|0)
- 1:   Hemoglobin M Disease [MESH:C581942](0|0) (0|0|0)
- 1:   Methemoglobinemia Type IV [MESH:C567102](0|0) (0|0|0)
- 1:   Methemoglobinemia, Alpha-Globin Type [MESH:C564194](0|0) (0|0|0)
- 1:   Methemoglobinemia, Beta-Globin Type [MESH:C564192](0|0) (0|0|0)
- 1:   NADH cytochrome B5 reductase deficiency [MESH:C537841](0|0) (0|0|0)