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Homocysteinemia MeSH Supplementary Concept Data 2024


MeSH Supplementary
Homocysteinemia
Unique ID
C566403
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566403
Heading Mapped to
*Hyperhomocysteinemia
Frequency
158
Note
Elevated serum HOMOCYSTEINE levels that occur in several inherited metabolic disorders. Germline mutations in the CBS gene (OMIM: 613381) have been identified for homocysitinuria, and in the MTHFR gene (OMIM: 607093) for N(5,10)-methylenetetrahydrofolate reductase deficiency. OMIM: 603174
Date of Entry
2012/11/05
Revision Date
2015/08/18
Homocysteinemia Preferred
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