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Disease Ontology (DO): congenital nervous system abnormality

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Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term (+ for parents, - for children) DO term [DO ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + 2:   disease [DOID:4] <8>
+ 1:   physical disorder [DOID:0080015] <20>(5|9) (6|0|1)
0:   congenital nervous system abnormality [DOID:2490] <5>(1|1) (1|0|0)
- 1:   holoprosencephaly [DOID:4621] <10>(0|0) (0|0|0)
- 1:   anencephaly [DOID:0060668] <1>(0|0) (0|0|0)
- 1:   lissencephaly [DOID:0050453] <1>(0|0) (0|0|0)
- 1:   microcephaly [DOID:10907](1|1) (1|0|0)
- 1:   periventricular nodular heterotopia [DOID:0050454](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)
p53-like transcription factors0.1089Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
T-box0.03327Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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)
p53-like transcription factors0.08668Inherited


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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