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Phenotypic Abnormality (PA): Abnormality of the corticospinal tract

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

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:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + 3:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + 2:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ 1:   Morphological abnormality of the pyramidal tract [HP:0002062] <2>(0|1) (0|0|0)
0:   Abnormality of the corticospinal tract [HP:0002492] <3>(0|1) (0|0|0)
- 1:   Atrophy/Degeneration involving the corticospinal tracts [HP:0007372] <2>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia involving the corticospinal tracts [HP:0007365] <1>(0|0) (0|0|0)
- 1:   Corticospinal tract pallor [HP:0008361](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Extended AAA-ATPase domain0.0003386Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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