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- Q994859 subject Q6902466.
- Q994859 subject Q7215445.
- Q994859 subject Q7215482.
- Q994859 subject Q8218498.
- Q994859 abstract "Classical homocystinuria, also known as cystathionine beta synthase deficiency or CBS deficiency, is an inherited disorder of the metabolism of the amino acid methionine, often involving cystathionine beta synthase. It is an inherited autosomal recessive trait, which means a child needs to inherit a copy of the defective gene from both parents to be affected.".
- Q994859 icd10 "E72.1".
- Q994859 icd9 "270.4".
- Q994859 meshId "D006712".
- Q994859 omim "236200".
- Q994859 thumbnail L-Homocysteine.svg?width=300.
- Q994859 wikiPageExternalLink viewer?a=v&pid=sites&srcid=ZGVmYXVsdGRvbWFpbnxtdWx0aWZhY3RvcmhlYWx0aHxneDoyMjRkY2I4NmI2MDZlNTc4.
- Q994859 wikiPageExternalLink diet.htm.
- Q994859 wikiPageExternalLink NBK1524.
- Q994859 wikiPageWikiLink Q1057.
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- Q994859 wikiPageWikiLink Q6902466.
- Q994859 wikiPageWikiLink Q7215445.
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- Q994859 wikiPageWikiLink Q8218498.
- Q994859 wikiPageWikiLink Q82682.
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- Q994859 icd "270.4".
- Q994859 icd "E72.1".
- Q994859 meshid "D006712".
- Q994859 name "Homocystinuria".
- Q994859 omim "236200".
- Q994859 type Disease.
- Q994859 type Thing.
- Q994859 type Q12136.
- Q994859 comment "Classical homocystinuria, also known as cystathionine beta synthase deficiency or CBS deficiency, is an inherited disorder of the metabolism of the amino acid methionine, often involving cystathionine beta synthase. It is an inherited autosomal recessive trait, which means a child needs to inherit a copy of the defective gene from both parents to be affected.".
- Q994859 label "Homocystinuria".
- Q994859 depiction L-Homocysteine.svg.
- Q994859 name "Homocystinuria".