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Phenotypic Abnormality (PA): Aplasia/Hypoplasia of the pyramidal tract

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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:   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)
+ 1:   Aplasia/Hypoplasia involving the central nervous system [HP:0002977] <13>(19|26) (23|13|3)
0:   Aplasia/Hypoplasia of the pyramidal tract [HP:0007363] <2>(0|0) (0|0|0)
- 1:   Aplasia of the pyramidal tract [HP:0100322](0|0) (0|0|0)
- 1:   Hypoplasia of the pyramidal tract [HP:0007348](0|0) (0|0|0)