SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Thyroid agenesis

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the endocrine system [HP:0000818] <16>(28|35) (35|13|5)
+ + + 3:   Abnormality of the thyroid gland [HP:0000820] <2>(8|7) (8|3|0)
+ + 2:   Abnormality of thyroid morphology [HP:0011772] <8>(7|6) (7|3|0)
+ 1:   Thyroid dysgenesis [HP:0008188] <4>(1|0) (1|0|0)
0:   Thyroid agenesis [HP:0008191](1|0) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain-like0.0008735Direct


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)
Homeodomain-like0.0004587Direct


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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