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Phenotypic Abnormality (PA): Vascular skin abnormality

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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:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + 3:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of skin morphology [HP:0011121] <22>(29|49) (40|31|11)
+ + 2:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ 1:   Generalized abnormality of skin [HP:0011354] <12>(8|12) (12|4|1)
+ 1:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
0:   Vascular skin abnormality [HP:0011276] <10>(6|10) (9|2|1)
- 1:   Erythema [HP:0010783] <7>(0|1) (1|0|0)
- 1:   Telangiectasia [HP:0001009] <6>(1|2) (1|0|0)
- 1:   Subcutaneous hemorrhage [HP:0001933] <3>(1|5) (3|0|1)
- 1:   Urticaria [HP:0001025] <3>(1|0) (1|0|0)
- 1:   Angiokeratoma [HP:0001014] <1>(1|0) (1|0|0)
- 1:   Prominent superficial blood vessels [HP:0007394] <1>(0|0) (0|0|0)
- 1:   Vasculitis in the skin [HP:0200029] <1>(0|0) (0|0|0)
- 1:   Angioedema [HP:0100665](0|0) (0|0|0)
- 1:   Cutis marmorata [HP:0000965](2|2) (2|0|0)
- 1:   Non-pruritic urticaria [HP:0011137](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
DNA/RNA polymerases0.01453Inherited
ARID-like0.01479Inherited
Integrin domains0.04272Inherited
DEATH domain0.05528Inherited
(Trans)glycosidases0.1106Inherited
HMG-box0.2518Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
ARID domain0.01113Inherited
Intermediate filament protein, coiled coil region0.01889Inherited
Discoidin domain (FA58C, coagulation factor 5/8 C-terminal domain)0.02776Inherited
VWC domain0.02776Inherited
DnaQ-like 3'-5' exonuclease0.02776Inherited
Integrin domains0.0338Inherited
DEATH domain, DD0.06141Inherited
Phoshoinositide 3-kinase (PI3K), catalytic domain0.1353Inherited
HMG-box0.2275Inherited
Ngr ectodomain-like0.3756Inherited


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)
DNA/RNA polymerases0.009631Inherited
ARID-like0.009821Inherited
Intermediate filament protein, coiled coil region0.01538Inherited
Integrin domains0.03088Inherited
DEATH domain0.04112Inherited
FnI-like domain0.05566Inherited
(Trans)glycosidases0.08728Inherited
HMG-box0.2151Inherited
L domain-like0.7807Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
47986,52540
  • 47986 - DEATH domain
  • 52540 - P-loop containing nucleoside triphosphate hydrolases
  • 0.0001674Direct
    57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.0009337Direct

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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
  • 0.005248Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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