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Phenotypic Abnormality (PA): Abnormal sclera morphology

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the eye [HP:0000478] <2>(64|78) (69|38|28)
+ 1:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
0:   Abnormal sclera morphology [HP:0000591] <12>(0|1) (1|0|0)
- 1:   Scleral staphyloma [HP:0030854] <2>(0|0) (0|0|0)
- 1:   Blue sclerae [HP:0000592](0|1) (1|0|0)
- 1:   Deep episcleral hyperemia [HP:0025340](0|0) (0|0|0)
- 1:   Episcleritis [HP:0100534](0|0) (0|0|0)
- 1:   Limbal dermoid [HP:0001140](0|0) (0|0|0)
- 1:   Ocular melanocytosis [HP:0025534](0|0) (0|0|0)
- 1:   Pigmentation of the sclera [HP:0007832](0|0) (0|0|0)
- 1:   Scleral rupture [HP:0025513](0|0) (0|0|0)
- 1:   Scleral schwannoma [HP:0100011](0|0) (0|0|0)
- 1:   Scleral thickening [HP:0030823](0|0) (0|0|0)
- 1:   Scleritis [HP:0100532](0|0) (0|0|0)
- 1:   Superficial episcleral hyperemia [HP:0025339](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
VWC domain0.001495Inherited


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)
Nucleotide-diphospho-sugar transferases0.007209Inherited


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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