FA complementation group I

Preferred Label : FA complementation group I;

Approved symbol HGNC : FANCI;

Alias symbols HGNC : FLJ10719;

Chromosome HGNC : 15q26.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000140525;

Details

Origin ID

HGNC:25568;

UMLS CUI

C1825278;

Automatic exact mappings (from CISMeF team)
- FA complementation group I [ORDO Gene]
- Fanci gene [OMIM gene]
- Fanconi anemia, complementation group I [OMIM Phenotype]
NCIt concept
- FANCI Gene [NCIt concept]
OMIM gene
- Fanci gene [OMIM gene]
Orphanet gene
- FA complementation group I [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FANCI Gene [NCIt concept]
- Fanci gene [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Details

Origin ID

HGNC:25568;

UMLS CUI

C1825278;

Automatic exact mappings (from CISMeF team)
- FA complementation group I [ORDO Gene]
- Fanci gene [OMIM gene]
- Fanconi anemia, complementation group I [OMIM Phenotype]
NCIt concept
- FANCI Gene [NCIt concept]
OMIM gene
- Fanci gene [OMIM gene]
Orphanet gene
- FA complementation group I [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FANCI Gene [NCIt concept]
- Fanci gene [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Details

Origin ID

HGNC:25568;

UMLS CUI

C1825278;

Automatic exact mappings (from CISMeF team)
- FA complementation group I [ORDO Gene]
- Fanci gene [OMIM gene]
- Fanconi anemia, complementation group I [OMIM Phenotype]
NCIt concept
- FANCI Gene [NCIt concept]
OMIM gene
- Fanci gene [OMIM gene]
Orphanet gene
- FA complementation group I [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FANCI Gene [NCIt concept]
- Fanci gene [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Details

Origin ID

HGNC:25568;

UMLS CUI

C1825278;

Automatic exact mappings (from CISMeF team)
- FA complementation group I [ORDO Gene]
- Fanci gene [OMIM gene]
- Fanconi anemia, complementation group I [OMIM Phenotype]
NCIt concept
- FANCI Gene [NCIt concept]
OMIM gene
- Fanci gene [OMIM gene]
Orphanet gene
- FA complementation group I [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FANCI Gene [NCIt concept]
- Fanci gene [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Details

Origin ID

HGNC:25568;

UMLS CUI

C1825278;

Automatic exact mappings (from CISMeF team)
- FA complementation group I [ORDO Gene]
- Fanci gene [OMIM gene]
- Fanconi anemia, complementation group I [OMIM Phenotype]
NCIt concept
- FANCI Gene [NCIt concept]
OMIM gene
- Fanci gene [OMIM gene]
Orphanet gene
- FA complementation group I [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FANCI Gene [NCIt concept]
- Fanci gene [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients