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Phenotypic Abnormality (PA): Central nervous system cyst

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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>(142|168) (156|103|45)
+ + 2:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ 1:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
0:   Central nervous system cyst [HP:0030724] <3>(2|1) (2|0|0)
- 1:   Intracranial cystic lesion [HP:0010576] <8>(2|1) (2|0|0)
- 1:   Neurenteric cyst [HP:0030725] <2>(0|0) (0|0|0)
- 1:   Tarlov cyst [HP:0025643](0|0) (0|0|0)


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

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARID-like0.001035Inherited
Nucleotide-diphospho-sugar transferases0.006228Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
ARID domain0.0005197Direct


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)
ARID-like0.0005514Direct
Nucleotide-diphospho-sugar transferases0.003854Inherited


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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