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Phenotypic Abnormality (PA): Aplasia/Hypoplasia of the eyelid

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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)
+ + + + + + + + 8:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + 7:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + 6:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + 5:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + + 4:   Abnormality of the orbital region [HP:0000315] <4>(17|24) (19|5|4)
+ + + 3:   Abnormality of the ocular adnexa [HP:0032039] <2>(17|24) (19|5|4)
+ + 2:   Abnormal ocular adnexa morphology [HP:0030669] <6>(17|24) (19|5|4)
+ 1:   Abnormal eyelid morphology [HP:0000492] <26>(10|17) (12|2|3)
0:   Aplasia/Hypoplasia of the eyelid [HP:0011226] <4>(1|1) (1|0|0)
- 1:   Eyelid coloboma [HP:0000625] <2>(0|0) (0|0|0)
- 1:   Hypoplasia of eyelid [HP:0430009] <2>(0|0) (0|0|0)
- 1:   Ablepharon [HP:0011224](0|0) (0|0|0)
- 1:   Cryptophthalmos [HP:0001126](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
CalX-like0.00005941Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
CalX-beta domain0.00004455Direct


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)
CalX-like0.00002685Direct


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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