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Phenotypic Abnormality (PA): Abnormality of the spinal cord

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the nervous system [HP:0000707] <4>(147|170) (164|102|45)
+ + 2:   Abnormality of nervous system morphology [HP:0012639] <5>(70|97) (81|48|16)
+ 1:   Morphological abnormality of the central nervous system [HP:0002011] <17>(61|85) (71|41|16)
0:   Abnormality of the spinal cord [HP:0002143] <16>(3|5) (3|0|2)
- 1:   Abnormal spinal meningeal morphology [HP:0010303] <6>(0|0) (0|0|0)
- 1:   Spinal cord lesion [HP:0100561] <6>(0|0) (0|0|0)
- 1:   Abnormal conus terminalis morphology [HP:0031938] <2>(0|0) (0|0|0)
- 1:   Abnormality of the dorsal column of the spinal cord [HP:0011397] <2>(0|0) (0|0|0)
- 1:   Myelopathy [HP:0002196] <2>(0|0) (0|0|0)
- 1:   Abnormality of the spinocerebellar tracts [HP:0003133] <1>(0|0) (0|0|0)
- 1:   Atrophy/Degeneration involving the spinal cord [HP:0007344] <1>(0|0) (0|0|0)
- 1:   Spinal cord compression [HP:0002176] <1>(0|0) (0|0|0)
- 1:   Spinal cord tumor [HP:0010302] <1>(0|0) (0|0|0)
- 1:   Spinal dysraphism [HP:0010301] <1>(3|5) (3|0|0)
- 1:   Cervicomedullary schisis [HP:0030325](0|0) (0|0|0)
- 1:   Hyperintensity of MRI T2 signal of the spinal cord [HP:0040272](0|0) (0|0|0)
- 1:   Long-tract signs [HP:0002423](0|0) (0|0|0)
- 1:   Myelitis [HP:0012486](0|0) (0|0|0)
- 1:   Spinal arteriovenous malformation [HP:0002390](0|0) (0|0|0)
- 1:   Spinal cord posterior columns myelin loss [HP:0008311](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
RuvA domain 2-like0.003081Inherited
ARID-like0.009844Inherited
Bromodomain0.0376Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
VWC domain0.0004006Direct
Ras-binding domain, RBD0.00213Inherited
ARID domain0.007813Inherited
Bromodomain0.03356Inherited
Protein kinase cysteine-rich domain (cys2, phorbol-binding domain)0.04554Inherited


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)
RuvA domain 2-like0.001821Inherited
ARID-like0.006413Inherited
Bromodomain0.02722Inherited

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57184,57196,57184
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0001773Direct
    57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0007024Direct


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