Wikidata

(Q994859)

English

homocystinuria

amino acid metabolic disorder that involves an accumulation of homocysteine in the serum and an increased excretion of homocysteine in the urine

  • CBS deficiency
  • Homocystinuria (disorder)
  • cystathionine beta synthase deficiency
  • cystathionine synthase deficiency
  • Homocystinuria
In more languages

Statements

health specialty
endocrinology
0 references
medical genetics
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Commons category
Homocystinuria
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Identifiers

NL CR AUT ID
ph180722
subject named as
homocystinurie
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MeSH descriptor ID
D006712
subject named as
Homocystinuria
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KEGG ID
H00183
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Mondo ID
MONDO_0004737
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