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hyperhomocysteinemia
Disease Summary
Associated Targets (14)
Tbio
7
Tchem
5
Tclin
1
Tdark
1
Mondo Description A serious metabolic condition caused by mutations in the MTHFR gene, medications, or nutritional deficiency. It results in increased levels of homocysteine in the blood. Patients with this condition are at an increased risk for recurrent blood clots formation and cardiovascular accidents.
Disease Ontology Description An amino acid metabolic disorder that involves an abnormally large level of homocysteine in the blood.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:9279
MESH:D020138
NCIT:C84770
SCTID:419503008
UMLS:C0598608
MONDO:0004743
High level summary of knowledge for a disease, including descriptions and datasource references.