Fumarate hydratase

Preferred Label : Fumarate hydratase;

Symbol : FH;

CISMeF acronym : FH;

Type : Gene;

Alternative titles and symbols : FUMARASE;

Included titles and symbols : Fumarate hydratase, cytosolic; Fumarate hydratase, mitochondrial; FH1; FH2;

Ensembl ID : ENSG00000091483;

Prefixed ID : *136850;

Details

Origin ID

136850;

UMLS CUI

C1366530;

Automatic exact mappings (from CISMeF team)
- CFH wt Allele [NCIt concept]
- FH Gene [NCIt concept]
- FH gene [LOINC component]
- Familial hyperaldosteronism [ORDO Disease]
- Familial hyperaldosteronism type 1 [ICD-11 More detail]
- Familial hyperaldosteronism type 2 [ICD-11 More detail]
- Familial hyperaldosteronism type I [ORDO Disease]
- Familial hyperaldosteronism type II [ORDO Disease]
- Family history with explicit context (situation) [SNOMED CT concept]
- Fumarase [LOINC component]
- Fumarate Hydratase, Mitochondrial [NCIt concept]
- Fumarate hydratase (substance) [SNOMED CT concept]
- Hyperlipoproteinemia, Type IIa [NCIt concept]
- LDLR wt Allele [NCIt concept]
- filamin B [ORDO Gene]
- fumarase A [MeSH concept]
- fumarate hydratase [ORDO Gene]
- fumarate hydratase [MeSH concept]
- fumarate hydratase [HGNC gene]
- fumarate hydratase [MeSH Descriptor]
- fumarate hydratase [SNOMED Notion]
- oxaloacetate tautomerase [MeSH Supplementary Concept]
HGNC gene
- fumarate hydratase [HGNC gene]
NCIt concept(s)
- FH Gene [NCIt concept]
- FH wt Allele [NCIt concept]
- Fumarate Hydratase, Mitochondrial [NCIt concept]
ORDO concept(s)
- fumarate hydratase [ORDO Gene]
Phenotypes related
- Fumarase deficiency [OMIM Phenotype]
- Hereditary leiomyomatosis and renal cell cancer [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FH Gene [NCIt concept]
- FH gene [LOINC component]
- fumarate hydratase [HGNC gene]

Keyword's position in hierarchy(ies) :

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