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Phenotypic Abnormality (PA): Abnormal facial shape

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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 head or neck [HP:0000152] <2>(87|107) (98|59|37)
+ + 2:   Abnormality of the head [HP:0000234] <6>(86|105) (97|58|37)
+ 1:   Abnormality of the face [HP:0000271] <14>(72|88) (83|47|30)
0:   Abnormal facial shape [HP:0001999] <16>(5|10) (6|1|0)
- 1:   Facial asymmetry [HP:0000324] <5>(0|0) (0|0|0)
- 1:   Large face [HP:0100729] <2>(1|2) (1|0|0)
- 1:   Small face [HP:0000274] <2>(2|3) (2|0|0)
- 1:   Coarse facial features [HP:0000280] <1>(1|3) (2|0|0)
- 1:   Facial shape deformation [HP:0011334] <1>(0|0) (0|0|0)
- 1:   Abnormality of the shape of the midface [HP:0430026](0|0) (0|0|0)
- 1:   Bird-like facies [HP:0000320](0|0) (0|0|0)
- 1:   Craniofacial disproportion [HP:0005461](0|0) (0|0|0)
- 1:   Doll-like facies [HP:0000295](0|0) (0|0|0)
- 1:   Elfin facies [HP:0004428](0|0) (0|0|0)
- 1:   Flat face [HP:0012368](0|0) (0|0|0)
- 1:   Moon facies [HP:0500011](0|0) (0|0|0)
- 1:   Oval face [HP:0000300](0|0) (0|0|0)
- 1:   Round face [HP:0000311](0|0) (0|1|0)
- 1:   Square face [HP:0000321](0|0) (0|0|0)
- 1:   Triangular face [HP:0000325](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Bromodomain0.0006375Direct
SNARE fusion complex0.003674Inherited
Tropomyosin0.04739Inherited
Alkaline phosphatase-like0.09771Inherited
Myosin rod fragments0.1599Inherited


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
beta-glycanases0Direct
Bromodomain0.0004191Direct
SNARE fusion complex0.002438Inherited
Arylsulfatase0.02597Inherited
Tropomyosin0.03787Inherited
Tandem AAA-ATPase domain0.04463Inherited
BCR-homology GTPase activation domain (BH-domain)0.04598Inherited
Clathrin coat assembly domain0.0554Inherited
Clathrin adaptor core protein0.1362Inherited
Myosin rod fragments0.1398Inherited


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)
Bromodomain0.0003357Direct
SNARE fusion complex0.002208Inherited
(Trans)glycosidases0.003655Inherited
Tropomyosin0.03508Inherited
Alkaline phosphatase-like0.07706Inherited
Myosin rod fragments0.1319Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.05192Inherited


    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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