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Phenotypic Abnormality (PA): Internal hemorrhage

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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:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormal cardiovascular system physiology [HP:0011025] <16>(21|34) (29|18|16)
+ + 2:   Abnormality of blood and blood-forming tissues [HP:0001871] <11>(24|35) (31|16|5)
+ 1:   Abnormality of blood circulation [HP:0011028] <3>(7|11) (11|3|1)
+ 1:   Abnormal bleeding [HP:0001892] <16>(8|15) (14|3|1)
0:   Internal hemorrhage [HP:0011029] <7>(7|11) (11|3|1)
- 1:   Intracranial hemorrhage [HP:0002170] <6>(3|5) (5|1|1)
- 1:   Gastrointestinal hemorrhage [HP:0002239] <5>(3|5) (4|1|0)
- 1:   Hemorrhage of the eye [HP:0011885] <5>(0|0) (0|0|0)
- 1:   Pulmonary hemorrhage [HP:0040223] <2>(0|0) (1|0|0)
- 1:   Antepartum hemorrhage [HP:0025328](0|0) (0|0|0)
- 1:   Joint hemorrhage [HP:0005261](2|2) (2|1|0)
- 1:   Muscle haemorrhage [HP:0040242](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-domain0.0000001714Direct
Fibrinogen C-terminal domain-like0.0002731Direct
Snake toxin-like0.006622Inherited
Integrin domains0.01436Inherited
Trypsin-like serine proteases0.2177Inherited
L domain-like0.4755Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
GLA-domain0.0000001356Direct
DNA gyrase/MutL, N-terminal domain0.00002366Direct
DNA gyrase/MutL, second domain0.00002366Direct
Fibrinogen C-terminal domain-like0.0002197Direct
Medium chain acyl-CoA dehydrogenase-like, C-terminal domain0.01216Inherited
Medium chain acyl-CoA dehydrogenase, NM (N-terminal and middle) domains0.01216Inherited
Integrin domains0.01216Inherited
Eukaryotic proteases0.2086Inherited
Ngr ectodomain-like0.2613Inherited
Second domain of FERM0.2613Inherited


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-domain0.00000006676Direct
Fibrinogen C-terminal domain-like0.0001338Direct
ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase0.001743Inherited
Snake toxin-like0.004135Inherited
Integrin domains0.009526Inherited
Cystine-knot cytokines0.1215Inherited
Trypsin-like serine proteases0.1836Inherited
Immunoglobulin0.2314Inherited
Second domain of FERM0.2436Inherited
L domain-like0.4317Inherited

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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
  • 0Direct
    55874,54211
  • 55874 - ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase
  • 54211 - Ribosomal protein S5 domain 2-like
  • 0.00001443Direct
    57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.6068Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57535,57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.2818Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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