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Phenotypic Abnormality (PA): Microphthalmia

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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 the eye [HP:0000478] <2>(64|78) (69|38|28)
+ + 2:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ 1:   Abnormality of globe size [HP:0100887] <3>(3|2) (3|1|0)
+ 1:   Aplasia/Hypoplasia affecting the eye [HP:0008056] <5>(4|4) (4|1|0)
0:   Microphthalmia [HP:0000568] <2>(3|2) (3|1|0)
- 1:   Bilateral microphthalmos [HP:0007633](0|0) (0|0|0)
- 1:   Unilateral microphthalmos [HP:0011480](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Restriction endonuclease-like0.0001264Direct
RuvA domain 2-like0.0001264Direct
CalX-like0.0004972Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
XPF/Rad1/Mus81 nuclease0Direct
CalX-beta domain0.0002508Direct


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)
Restriction endonuclease-like0.00005907Direct
RuvA domain 2-like0.00005907Direct
CalX-like0.0002515Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
52980,47781
  • 52980 - Restriction endonuclease-like
  • 47781 - RuvA domain 2-like
  • 0Direct


    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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