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Phenotypic Abnormality (PA): Developmental regression

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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:   Neurodevelopmental abnormality [HP:0012759] <5>(34|50) (39|26|11)
0:   Developmental regression [HP:0002376](0|3) (0|1|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
IF2B-like0Direct
DNA gyrase/MutL, second domain0.00001564Direct
DNA gyrase/MutL, N-terminal domain0.00001564Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
55874,54211
  • 55874 - ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase
  • 54211 - Ribosomal protein S5 domain 2-like
  • 0.00001535Direct