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Disease Ontology (DO): amino acid metabolic disorder

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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)
+ + + 3:   disease [DOID:4] <8>
+ + 2:   disease of metabolism [DOID:0014667] <2>(22|34) (27|12|5)
+ 1:   inherited metabolic disorder [DOID:655] <18>(12|15) (16|5|0)
0:   amino acid metabolic disorder [DOID:9252] <30>(1|1) (1|0|0)
- 1:   organic acidemia [DOID:0060159] <5>(0|0) (0|0|0)
- 1:   serine deficiency [DOID:0050721] <5>(0|0) (0|0|0)
- 1:   cerebral creatine deficiency syndrome [DOID:0050798] <3>(0|0) (0|0|0)
- 1:   gamma-amino butyric acid metabolism disorder [DOID:0060176] <3>(0|0) (0|0|0)
- 1:   hypermethioninemia [DOID:0050544] <3>(0|0) (0|0|0)
- 1:   tyrosinemia [DOID:9275] <3>(0|0) (0|0|0)
- 1:   urea cycle disorder [DOID:9267] <3>(0|0) (0|0|0)
- 1:   2-hydroxyglutaric aciduria [DOID:0050573] <2>(0|0) (0|0|0)
- 1:   multiple carboxylase deficiency [DOID:857] <2>(0|0) (0|0|0)
- 1:   histidine metabolism disease [DOID:9265] <1>(0|0) (0|0|0)
- 1:   3-Methylcrotonyl-CoA carboxylase deficiency [DOID:0050710](0|0) (0|0|0)
- 1:   Bh4-deficient hyperphenylalaninemia A [DOID:0090106](0|0) (0|0|0)
- 1:   Brunner Syndrome [DOID:0060693](0|0) (0|0|0)
- 1:   Hartnup disease [DOID:1060](0|0) (0|0|0)
- 1:   adenine phosphoribosyltransferase deficiency [DOID:0060350](0|0) (0|0|0)
- 1:   adenylosuccinase lyase deficiency [DOID:0050762](0|0) (0|0|0)
- 1:   alkaptonuria [DOID:9270](0|0) (0|0|0)
- 1:   argininosuccinic aciduria [DOID:14755](0|0) (0|0|0)
- 1:   carbamoyl phosphate synthetase I deficiency disease [DOID:9280](0|0) (0|0|0)
- 1:   cystathioninuria [DOID:0090142](0|0) (0|0|0)
- 1:   cystinuria [DOID:9266](0|0) (0|0|0)
- 1:   dicarboxylic aminoaciduria [DOID:0060650](0|0) (0|0|0)
- 1:   glycine encephalopathy [DOID:9268](0|0) (0|0|0)
- 1:   homocystinuria [DOID:9263](0|0) (0|0|0)
- 1:   hyperhomocysteinemia [DOID:9279](1|1) (1|0|0)
- 1:   hyperlysinemia [DOID:9274](0|0) (0|0|0)
- 1:   lysinuric protein intolerance [DOID:0060439](0|0) (0|0|0)
- 1:   ornithine translocase deficiency [DOID:0050720](0|0) (0|0|0)
- 1:   phenylketonuria [DOID:9281](0|0) (0|0|0)
- 1:   systemic primary carnitine deficiency disease [DOID:14365](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Homocysteine S-methyltransferase0Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Homocysteine S-methyltransferase0Direct


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)
Homocysteine S-methyltransferase0Direct


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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