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Disease Ontology (DO): hypothyroidism

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Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term (+ for parents, - for children) DO term [DO ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   disease [DOID:4] <8>
+ + + 3:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + 2:   endocrine system disease [DOID:28] <7>(14|16) (15|4|1)
+ 1:   thyroid gland disease [DOID:50] <10>(4|3) (4|1|0)
0:   hypothyroidism [DOID:1459] <6>(3|1) (3|0|0)
- 1:   Bamforth-Lazarus syndrome [DOID:0050655](0|0) (0|0|0)
- 1:   congenital hypothyroidism [DOID:0050328](0|0) (0|0|0)
- 1:   iodine hypothyroidism [DOID:5083](0|0) (0|0|0)
- 1:   myxedema [DOID:11634](0|0) (0|0|0)
- 1:   postsurgical hypothyroidism [DOID:1458](0|0) (0|0|0)
- 1:   thyroid hormone resistance syndrome [DOID:11633](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Ferredoxin reductase-like, C-terminal NADP-linked domain0.00003278Direct
Riboflavin synthase domain-like0.00003278Direct
Thyroglobulin type-1 domain0.00005515Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Thyroglobulin type-1 domain0.00004301Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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)
Riboflavin synthase domain-like0.00001867Direct
Ferredoxin reductase-like, C-terminal NADP-linked domain0.00001867Direct
Thyroglobulin type-1 domain0.00003185Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
(show help)