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Phenotypic Abnormality (PA): Abnormality of the pons

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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)
+ + + + 4:   Abnormality of nervous system morphology [HP:0012639] <5>(70|97) (81|48|16)
+ + + 3:   Morphological abnormality of the central nervous system [HP:0002011] <17>(61|85) (71|41|16)
+ + 2:   Abnormality of brain morphology [HP:0012443] <13>(44|63) (54|31|14)
+ + 2:   Abnormality of hindbrain morphology [HP:0011282] <2>(5|6) (7|2|1)
+ 1:   Abnormality of the metencephalon [HP:0011283] <3>(5|6) (7|2|1)
+ 1:   Abnormality of brainstem morphology [HP:0002363] <10>(3|2) (3|1|0)
0:   Abnormality of the pons [HP:0007361] <4>(1|0) (1|0|0)
- 1:   Abnormality of the superior cerebellar peduncle [HP:0011932] <4>(0|0) (0|0|0)
- 1:   Hypoplasia of the pons [HP:0012110] <1>(1|0) (1|0|0)
- 1:   Hypoplasia of the ventral pons [HP:0006850](0|0) (0|0|0)
- 1:   Pontine tegmental cap [HP:0030975](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Nucleotide-diphospho-sugar transferases0.003931Inherited


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)
Nucleotide-diphospho-sugar transferases0.002379Inherited


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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