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Disease Ontology (DO): Ehlers-Danlos syndrome

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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)
+ + + + + 5:   disease [DOID:4] <8>
+ + + + 4:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + 3:   musculoskeletal system disease [DOID:17] <3>(29|42) (37|17|6)
+ + 2:   connective tissue disease [DOID:65] <22>(23|31) (28|11|4)
+ 1:   collagen disease [DOID:854] <5>(7|11) (8|2|1)
0:   Ehlers-Danlos syndrome [DOID:13359] <6>(1|1) (1|0|0)
- 1:   Ehlers-Danlos syndrome progeroid type [DOID:0050802](0|0) (0|0|0)
- 1:   autosomal dominant type IV Ehlers-Danlos syndrome [DOID:14756](0|0) (0|0|0)
- 1:   autosomal recessive type IV Ehlers-Danlos syndrome [DOID:14759](0|0) (0|0|0)
- 1:   brittle cornea syndrome [DOID:14775](0|0) (0|0|0)
- 1:   type I Ehlers-Danlos syndrome [DOID:14720](0|0) (0|0|0)
- 1:   type III Ehlers-Danlos syndrome [DOID:14757](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
FnI-like domain0.0009142Direct


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
VWC domain0.00009792Direct


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)
FnI-like domain0.0005726Direct


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