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Phenotypic Abnormality (PA): Gait disturbance

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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 physiology [HP:0012638] <26>(104|120) (119|81|38)
+ 1:   Abnormality of movement [HP:0100022] <19>(26|25) (28|13|2)
0:   Gait disturbance [HP:0001288] <22>(6|6) (10|2|1)
- 1:   Dystonic gait [HP:0031954] <2>(0|0) (0|0|0)
- 1:   Gait ataxia [HP:0002066] <2>(0|0) (0|0|0)
- 1:   Spastic gait [HP:0002064] <2>(0|0) (0|0|0)
- 1:   Inability to walk [HP:0002540] <1>(0|0) (0|0|0)
- 1:   Shuffling gait [HP:0002362] <1>(0|0) (0|1|0)
- 1:   Unsteady gait [HP:0002317] <1>(1|1) (1|0|0)
- 1:   Antalgic gait [HP:0031955](0|0) (0|0|0)
- 1:   Broad-based gait [HP:0002136](0|0) (0|0|0)
- 1:   Cautious gait [HP:0031953](0|0) (0|0|0)
- 1:   Cerebellar ataxia associated with quadrupedal gait [HP:0009878](0|0) (0|0|0)
- 1:   Difficulty walking [HP:0002355](1|1) (2|0|0)
- 1:   Difficulty walking backward [HP:0031847](0|0) (0|0|0)
- 1:   Falls [HP:0002527](0|0) (0|0|0)
- 1:   Freezing of gait [HP:0031825](0|0) (0|0|0)
- 1:   Gait apraxia [HP:0010521](0|0) (0|0|0)
- 1:   Gait imbalance [HP:0002141](0|0) (0|0|0)
- 1:   Impaired tandem gait [HP:0031629](0|0) (0|0|0)
- 1:   Neurogenic claudication [HP:0031952](0|0) (0|0|0)
- 1:   Steppage gait [HP:0003376](0|0) (1|0|0)
- 1:   Tip-toe gait [HP:0030051](0|0) (0|0|0)
- 1:   Toe walking [HP:0040083](0|0) (0|0|1)
- 1:   Waddling gait [HP:0002515](1|2) (2|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
S15/NS1 RNA-binding domain0Direct
Lamin A/C globular tail domain0Direct
HIT-like0Direct
POZ domain0.1029Inherited
NagB/RpiA/CoA transferase-like0.1117Inherited
Tropomyosin0.157Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
a tRNA synthase domain0Direct
Lamin A/C globular tail domain0Direct
IF2B-like0Direct
Tropomyosin0.1217Inherited
Clathrin adaptor core protein0.1373Inherited
Myosin rod fragments0.2088Inherited


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)
HIT-like0Direct
S15/NS1 RNA-binding domain0Direct
Lamin A/C globular tail domain0Direct
ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase0.000727Direct
GST C-terminal domain-like0.002772Inherited
POZ domain0.0814Inherited
NagB/RpiA/CoA transferase-like0.08887Inherited
Tropomyosin0.1294Inherited
HSP20-like chaperones0.1381Inherited
Myosin rod fragments0.22Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
47060,55681
  • 47060 - S15/NS1 RNA-binding domain
  • 55681 - Class II aaRS and biotin synthetases
  • 0Direct
    48371,48371
  • 48371 - ARM repeat
  • 48371 - ARM repeat
  • 0.1369Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    46966,46966,46966
  • 46966 - Spectrin repeat
  • 46966 - Spectrin repeat
  • 46966 - Spectrin repeat
  • 0.2456Inherited


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