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Phenotypic Abnormality (PA): Inflammatory abnormality of the skin

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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 immune system [HP:0002715] <3>(38|52) (40|29|16)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + 3:   Abnormality of immune system physiology [HP:0010978] <14>(29|37) (31|22|11)
+ + 2:   Abnormal inflammatory response [HP:0012647] <2>(17|20) (18|11|3)
+ + 2:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ 1:   Increased inflammatory response [HP:0012649] <27>(15|18) (16|9|3)
+ 1:   Abnormality of skin physiology [HP:0011122] <6>(3|6) (5|3|0)
0:   Inflammatory abnormality of the skin [HP:0011123] <17>(3|4) (4|3|0)
- 1:   Skin rash [HP:0000988] <6>(0|2) (1|1|0)
- 1:   Eczema [HP:0000964] <5>(0|0) (0|0|0)
- 1:   Cutaneous abscess [HP:0031292] <3>(0|0) (0|0|0)
- 1:   Recurrent skin infections [HP:0001581] <3>(1|1) (1|0|0)
- 1:   Acne [HP:0001061] <2>(0|0) (0|0|0)
- 1:   Folliculitis [HP:0025084] <2>(0|0) (0|0|0)
- 1:   Neutrophilic infiltration of the skin [HP:0031234] <2>(0|0) (0|0|0)
- 1:   Erythroderma [HP:0001019] <1>(0|0) (0|0|0)
- 1:   Pustule [HP:0200039] <1>(0|0) (0|0|0)
- 1:   Crusting erythematous dermatitis [HP:0007473](0|0) (0|0|0)
- 1:   Deep dermal perivascular inflammatory infiltrate [HP:0031191](0|0) (0|0|0)
- 1:   Eosinophilic dermal infiltration [HP:0032022](0|0) (0|0|0)
- 1:   Erysipelas [HP:0001055](0|0) (0|0|0)
- 1:   Erythema nodosum [HP:0012219](0|0) (0|0|0)
- 1:   Perifolliculitis [HP:0012322](0|0) (0|0|0)
- 1:   Psoriasiform dermatitis [HP:0003765](1|1) (1|1|0)
- 1:   Superficial dermal perivascular inflammatory infiltrate [HP:0031190](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
DEATH domain0.00006593Direct
MHC antigen-recognition domain0.0274Inherited
SH2 domain0.1672Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Proteasome subunits0Direct
MHC antigen-recognition domain0.02214Inherited
Pyrin domain, PYD0.08347Inherited
SH2 domain0.154Inherited


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)
DEATH domain0.00002984Direct
N-terminal nucleophile aminohydrolases (Ntn hydrolases)0.0007264Direct
MHC antigen-recognition domain0.01909Inherited
SH2 domain0.1375Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
64268,50044
  • 64268 - PX domain
  • 50044 - SH3-domain
  • 0Direct
    47986,52540
  • 47986 - DEATH domain
  • 52540 - P-loop containing nucleoside triphosphate hydrolases
  • 0.0000516Direct
    54452,48726
  • 54452 - MHC antigen-recognition domain
  • 48726 - Immunoglobulin
  • 0.01909Inherited


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