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CTD Diseases (CD): Melanoma

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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:   Neoplasms, Germ Cell and Embryonal [MESH:D009373] <14>(10|14) (12|9|8)
+ + + 3:   Neoplasms, Nerve Tissue [MESH:D009380] <3>(10|15) (12|9|8)
+ + + 3:   Neoplasms [MESH:D009369] <18>(68|96) (74|65|31)
+ + 2:   Neuroectodermal Tumors [MESH:D017599] <4>(10|14) (12|9|8)
+ + 2:   Neoplasms by Histologic Type [MESH:D009370] <14>(45|58) (49|32|21)
+ 1:   Neuroendocrine Tumors [MESH:D018358] <11>(1|1) (1|1|0)
+ 1:   Nevi and Melanomas [MESH:D018326] <2>(1|2) (1|1|0)
0:   Melanoma [MESH:D008545] <9>(0|0) (0|1|0)
- 1:   Melanoma, Cutaneous Malignant [MESH:C562393] <10>(0|0) (0|0|0)
- 1:   Hutchinson's Melanotic Freckle [MESH:D018327](0|0) (0|0|0)
- 1:   Melanoma astrocytoma syndrome [MESH:C536149](0|0) (0|0|0)
- 1:   Melanoma, Amelanotic [MESH:D018328](0|0) (0|0|0)
- 1:   Melanoma, Experimental [MESH:D008546](0|0) (0|0|0)
- 1:   Melanoma, Malignant Familial Intraocular [MESH:C563596](0|0) (0|0|0)
- 1:   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985](0|0) (0|0|0)
- 1:   Primary malignant melanoma of the cervix [MESH:C536417](0|0) (0|0|0)
- 1:   Uveal melanoma [MESH:C536494](0|0) (0|0|0)

Supra-domain (Single|Duplex|Triple)

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Supra-domain (Duplex) in N- to C-terminal order

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
63748,63748
  • 63748 - Tudor/PWWP/MBT
  • 63748 - Tudor/PWWP/MBT
  • 0.0005907Direct

    LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm