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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> #Domains
(Superfamily|Family)
#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)

Superfamily

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Superfamily

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SCOP term FDR (all) Annotation (direct or inherited)
Homeodomain-like0.0008729Direct

LINKTO: Domain2BO Download and Domain2BO Algorithm

Supra-domain (Single|Duplex|Triple)

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Supra-domain (Single)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Homeodomain-like0.0004576Direct

LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm

Distribution on sTOL

Plot distribution on species Tree Of Life (sTOL) for Superfamily and/or Family domains annotated by this HP term
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Plot distribution on species Tree Of Life (sTOL) for single supra-domains annotated by this HP term
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