Filamin a - CISMeF

Preferred Label : Filamin a;

Symbol : FLNA;

CISMeF acronym : FLNA;

Type : Gene;

Alternative titles and symbols : Filamin, alpha; Filamin 1; Actin-binding protein 280; FLN1; FLN; ABP280;

Ensembl ID : ENSG00000196924;

Prefixed ID : *300017;

Details

Origin ID

300017;

UMLS CUI

C1414635;

Automatic exact mappings (from CISMeF team)
- FLNA Gene [NCIt concept]
- FLNA gene [LOINC component]
- FLNA wt Allele [NCIt concept]
- FLNC wt Allele [NCIt concept]
- Filamin [FMA entity]
- Filamin-A [NCIt concept]
- filamin A [ORDO Gene]
- filamin A [HGNC gene]
- filamin A [MeSH concept]
- filamin C [ORDO Gene]
- filamins [MeSH concept]
- filamins [MeSH Descriptor]
HGNC gene
- filamin A [HGNC gene]
NCIt concept(s)
- FLNA Gene [NCIt concept]
- FLNA wt Allele [NCIt concept]
- Filamin-A [NCIt concept]
ORDO concept(s)
- filamin A [ORDO Gene]
Phenotypes related
- Cardiac valvular dysplasia, X-linked [OMIM Phenotype]
- Fg syndrome 2 [OMIM Phenotype]
- Frontometaphyseal dysplasia 1 [OMIM Phenotype]
- Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked [OMIM Phenotype]
- Melnick-needles syndrome [OMIM Phenotype]
- Otopalatodigital syndrome, type I [OMIM Phenotype]
- Otopalatodigital syndrome, type II [OMIM Phenotype]
- Periventricular nodular heterotopia 1 [OMIM Phenotype]
- Terminal osseous dysplasia [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FLNA Gene [NCIt concept]
- FLNA gene [LOINC component]
- filamin A [HGNC gene]

Keyword's position in hierarchy(ies) :

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