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Phenotypic Abnormality (PA): Intracranial 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)
+ + + + + 5:   Abnormality of the nervous system [HP:0000707] <4>(147|170) (164|102|45)
+ + + + 4:   Abnormality of nervous system morphology [HP:0012639] <5>(70|97) (81|48|16)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the cardiovascular system [HP:0001626] <5>(59|81) (72|39|29)
+ + + 3:   Morphological abnormality of the central nervous system [HP:0002011] <17>(61|85) (71|41|16)
+ + + 3:   Abnormal cardiovascular system physiology [HP:0011025] <16>(21|32) (30|17|14)
+ + + 3:   Abnormality of blood and blood-forming tissues [HP:0001871] <11>(22|35) (29|15|5)
+ + 2:   Abnormality of blood circulation [HP:0011028] <3>(7|11) (12|3|1)
+ + 2:   Abnormality of brain morphology [HP:0012443] <13>(44|63) (54|31|14)
+ + 2:   Abnormality of the vasculature [HP:0002597] <13>(33|53) (44|26|18)
+ + 2:   Abnormal bleeding [HP:0001892] <16>(8|15) (15|3|1)
+ 1:   Abnormality of the cerebral vasculature [HP:0100659] <7>(7|10) (11|4|1)
+ 1:   Internal hemorrhage [HP:0011029] <7>(7|11) (12|3|1)
0:   Intracranial hemorrhage [HP:0002170] <6>(3|5) (6|1|1)
- 1:   Cerebral hemorrhage [HP:0001342] <2>(1|2) (3|1|1)
- 1:   Intraventricular hemorrhage [HP:0030746] <1>(0|0) (0|0|0)
- 1:   Cerebellar hemorrhage [HP:0011695](0|0) (0|0|0)
- 1:   Epidural hemorrhage [HP:0100310](0|0) (0|0|0)
- 1:   Subarachnoid hemorrhage [HP:0002138](2|1) (2|0|0)
- 1:   Subdural hemorrhage [HP:0100309](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
Integrin domains0.001141Inherited
Snake toxin-like0.04402Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
Medium chain acyl-CoA dehydrogenase, NM (N-terminal and middle) domains0.0008804Direct
Integrin domains0.0008804Direct
Medium chain acyl-CoA dehydrogenase-like, C-terminal domain0.0008804Direct
Second domain of FERM0.006995Inherited


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
Integrin domains0.0006268Direct
Cystine-knot cytokines0.0008715Direct
Second domain of FERM0.007755Inherited
Snake toxin-like0.0323Inherited
Complement control module/SCR domain0.08487Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.08487Inherited

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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
  • 0.08487Inherited


    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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