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Phenotypic Abnormality (PA): Abnormality of thyroid physiology

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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 endocrine system [HP:0000818] <16>(28|35) (35|13|5)
+ 1:   Abnormality of the thyroid gland [HP:0000820] <2>(8|7) (8|3|0)
0:   Abnormality of thyroid physiology [HP:0002926] <9>(1|1) (2|0|0)
- 1:   Hyperthyroidism [HP:0000836] <5>(0|0) (0|0|0)
- 1:   Hypothyroidism [HP:0000821] <4>(1|1) (2|0|0)
- 1:   Abnormal thyroid hormone level [HP:0031508] <3>(0|0) (0|0|0)
- 1:   Abnormal radioactive iodine uptake test result [HP:0031221] <2>(0|0) (0|0|0)
- 1:   Impaired sensitivity to thyroid stimulating hormone [HP:0011789] <2>(0|0) (0|0|0)
- 1:   Euthyroid hyperthyroxinemia [HP:0008247](0|0) (0|0|0)
- 1:   Impaired sensitivity to thyroid hormone [HP:0002930](0|0) (0|0|0)
- 1:   Positive perchlorate discharge test [HP:0025482](0|0) (0|0|0)
- 1:   Thyroid defect in oxidation and organification of iodide [HP:0008263](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
SAND domain-like0.0002922Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain0.03461Inherited


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)
SAND domain-like0.0001439Direct
Homeodomain-like0.02198Inherited


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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