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Phenotypic Abnormality (PA): Cerebellar hypoplasia

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the nervous system [HP:0000707] <4>(147|170) (164|102|45)
+ + + + + 5:   Abnormality of brain morphology [HP:0012443] <13>(44|63) (54|31|14)
+ + + + 4:   Abnormality of nervous system morphology [HP:0012639] <5>(70|97) (81|48|16)
+ + + + 4:   Abnormality of hindbrain morphology [HP:0011282] <2>(5|6) (7|2|1)
+ + + 3:   Morphological abnormality of the central nervous system [HP:0002011] <17>(61|85) (71|41|16)
+ + + 3:   Abnormality of the metencephalon [HP:0011283] <3>(5|6) (7|2|1)
+ + 2:   Abnormal cerebellum morphology [HP:0001317] <15>(5|6) (7|2|1)
+ + 2:   Aplasia/Hypoplasia involving the central nervous system [HP:0002977] <13>(18|22) (22|10|2)
+ 1:   Aplasia/Hypoplasia of the cerebellum [HP:0007360] <2>(0|1) (1|1|0)
0:   Cerebellar hypoplasia [HP:0001321] <2>(0|1) (1|1|0)
- 1:   Cerebellar hemisphere hypoplasia [HP:0100307](0|0) (0|0|0)
- 1:   Olivopontocerebellar hypoplasia [HP:0006955](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
MIR domain0.0006394Direct


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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)
MIR domain0.0008406Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
52374,47323
  • 52374 - Nucleotidylyl transferase
  • 47323 - Anticodon-binding domain of a subclass of class I aminoacyl-tRNA synthetases
  • 0.0008406Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
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