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Phenotypic Abnormality (PA): Edema

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of metabolism/homeostasis [HP:0001939] <16>(76|83) (79|38|16)
+ + 2:   Abnormal homeostasis [HP:0012337] <8>(42|43) (42|21|8)
+ 1:   Abnormality of fluid regulation [HP:0011032] <2>(8|8) (7|2|1)
0:   Edema [HP:0000969] <25>(8|8) (7|2|1)
- 1:   Pleural effusion [HP:0002202] <4>(1|0) (1|0|0)
- 1:   Hydrops fetalis [HP:0001789] <2>(0|0) (0|0|0)
- 1:   Lymphedema [HP:0001004] <2>(0|0) (0|0|0)
- 1:   Facial edema [HP:0000282] <1>(0|0) (0|0|0)
- 1:   Generalized edema [HP:0007430] <1>(1|1) (1|1|1)
- 1:   Increased nuchal translucency [HP:0010880] <1>(0|0) (0|0|0)
- 1:   Intestinal edema [HP:0005225] <1>(0|0) (0|0|0)
- 1:   Macular edema [HP:0040049] <1>(1|0) (0|0|0)
- 1:   Pedal edema [HP:0010741] <1>(0|0) (0|0|0)
- 1:   Angioedema [HP:0100665](0|0) (0|0|0)
- 1:   Cerebral edema [HP:0002181](0|0) (0|0|0)
- 1:   Corneal stromal edema [HP:0012040](0|0) (0|0|0)
- 1:   Edema of the dorsum of hands [HP:0007514](0|0) (0|0|0)
- 1:   Edema of the upper limbs [HP:0010742](0|0) (0|0|0)
- 1:   Genital edema [HP:0031188](0|0) (0|0|0)
- 1:   Hyperkeratosis over edematous areas [HP:0007448](0|0) (0|0|0)
- 1:   Hypoproteinemic edema [HP:0007609](0|0) (0|0|0)
- 1:   Joint swelling [HP:0001386](2|2) (2|0|0)
- 1:   Laryngeal edema [HP:0012027](0|0) (0|0|0)
- 1:   Muscular edema [HP:0100748](0|0) (0|0|0)
- 1:   Peau d'orange [HP:0025533](0|0) (0|0|0)
- 1:   Peripheral edema [HP:0012398](0|0) (0|0|0)
- 1:   Pharyngeal edema [HP:0011855](0|0) (0|0|0)
- 1:   Pulmonary edema [HP:0100598](0|0) (0|0|0)
- 1:   Tongue edema [HP:0040315](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Smc hinge domain0Direct
Fibrinogen coiled-coil and central regions0Direct
Ras GEF0.0002138Direct
MHC antigen-recognition domain0.0004223Direct
Fibrinogen C-terminal domain-like0.0565Inherited
Complement control module/SCR domain0.05984Inherited
4-helical cytokines0.09027Inherited
SCOP hierarchy in SUPERFAMILY0.5975Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Smc hinge domain0Direct
alpha-Amylases, C-terminal beta-sheet domain0Direct
Fibrinogen coiled-coil and central regions0Direct
Ras GEF0.000147Direct
MHC antigen-recognition domain0.0003166Direct
Ras-binding domain, RBD0.0006615Direct
Fibrinogen C-terminal domain-like0.04947Inherited
Complement control module/SCR domain0.05512Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Smc hinge domain0Direct
Fibrinogen coiled-coil and central regions0Direct
Ras GEF0.0001066Direct
MHC antigen-recognition domain0.0002177Direct
Fibrinogen C-terminal domain-like0.04252Inherited
Complement control module/SCR domain0.04532Inherited
4-helical cytokines0.07063Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
54452,48726
  • 54452 - MHC antigen-recognition domain
  • 48726 - Immunoglobulin
  • 0.0002177Direct
    57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.0248Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57535,57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.04252Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
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