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Disease Ontology (DO): inherited blood coagulation disease

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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:   hematopoietic system disease [DOID:74] <7>(27|29) (27|15|8)
+ 1:   blood coagulation disease [DOID:1247] <4>(16|18) (17|10|6)
0:   inherited blood coagulation disease [DOID:2214] <27>(6|6) (6|1|0)
- 1:   von Willebrand's disease [DOID:12531] <3>(0|0) (0|0|0)
- 1:   Bernard-Soulier syndrome [DOID:2217] <1>(1|1) (1|0|0)
- 1:   Glanzmann's thrombasthenia [DOID:2219](1|1) (1|0|0)
- 1:   Quebec platelet disorder [DOID:0111050](0|0) (0|0|0)
- 1:   Scott syndrome [DOID:0111052](0|0) (0|0|0)
- 1:   antithrombin III deficiency [DOID:3755](0|0) (0|0|0)
- 1:   congenital afibrinogenemia [DOID:2236](2|2) (2|0|0)
- 1:   factor V deficiency [DOID:2216](0|0) (0|0|0)
- 1:   factor VII deficiency [DOID:2215](0|0) (0|0|0)
- 1:   factor X deficiency [DOID:2222](0|0) (0|0|0)
- 1:   factor XIII deficiency [DOID:2211](0|0) (0|0|0)
- 1:   gray platelet syndrome [DOID:0111044](0|0) (0|0|0)
- 1:   hemophilia B [DOID:12259](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 10 [DOID:0111046](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 11 [DOID:0111057](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 12 [DOID:0111058](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 14 [DOID:0111047](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 15 [DOID:0111053](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 16 [DOID:0060691](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 17 [DOID:0111049](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 18 [DOID:0111051](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 19 [DOID:0111048](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 20 [DOID:0111055](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 3 [DOID:0111056](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 8 [DOID:0060692](0|0) (0|0|0)
- 1:   platelet-type bleeding disorder 9 [DOID:0111045](0|0) (0|0|0)
- 1:   protein C deficiency [DOID:3756](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
GLA-domain0.00003779Direct
Trypsin-like serine proteases0.0009167Direct
L domain-like0.004274Inherited
Fibrinogen C-terminal domain-like0.004274Inherited
Integrin domains0.004274Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
GLA-domain0.00002756Direct
Ngr ectodomain-like0.0003166Direct
Eukaryotic proteases0.0006963Direct
Fibrinogen C-terminal domain-like0.00317Inherited
Integrin domains0.00317Inherited


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)
Fibrinogen coiled-coil and central regions0Direct
GLA-domain0.00002157Direct
Trypsin-like serine proteases0.0005746Direct
Fibrinogen C-terminal domain-like0.00288Inherited
L domain-like0.00288Inherited
Integrin domains0.00288Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57630,57196
  • 57630 - GLA-domain
  • 57196 - EGF/Laminin
  • 0.000592Direct


    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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