Filamin b - CISMeF

Preferred Label : Filamin b;

Symbol : FLNB;

CISMeF acronym : FLNB;

Type : Gene;

Alternative titles and symbols : Filamin, beta; Actin-binding protein 276/278; ABP276/278;

Included titles and symbols : Truncated actin-binding protein; Actin-binding protein, truncated; Filamin homolog 1; TABP; FH1;

Ensembl ID : ENSG00000136068;

Prefixed ID : *603381;

Details

Origin ID

603381;

UMLS CUI

C1414636;

Automatic exact mappings (from CISMeF team)
- Familial hyperaldosteronism type 1 [ICD-11 More detail]
- Familial hyperaldosteronism type I [ORDO Disease]
- filamin B [ORDO Gene]
- filamin B [HGNC gene]
- filamin B [MeSH concept]
- filamins [MeSH Descriptor]
HGNC gene
- filamin B [HGNC gene]
ORDO concept(s)
- filamin B [ORDO Gene]
Phenotypes related
- Atelosteogenesis, type I [OMIM Phenotype]
- Atelosteogenesis, type III [OMIM Phenotype]
- Boomerang dysplasia [OMIM Phenotype]
- Larsen syndrome [OMIM Phenotype]
- Spondylocarpotarsal synostosis syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- filamin B [HGNC gene]

Keyword's position in hierarchy(ies) :

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