Fanconi Anemia, Complementation Group G

Preferred Label : Fanconi Anemia, Complementation Group G;

NCIt definition : Fanconi anemia caused by mutations of the FANCG gene.;

Origin ID

C125708;

UMLS CUI

C3469527;

Automatic exact mappings (from CISMeF team)
- FA complementation group G [ORDO Gene]
Currated CISMeF NLP mapping
- Fanconi anemia complementation group G [DO Concept]
- Fanconi anemia, complementation group g [OMIM Phenotype]
Has associated anatomic sites
- Bone Marrow [NCIt concept]
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Fanconi anemia complementation group G [DO Concept]
- Fanconi anemia, complementation group g [OMIM Phenotype]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_associated_disease
- Anemia [NCIt concept]
disease_has_finding
- Bone Marrow Failure [NCIt concept]
- Hereditary Lesion [NCIt concept]
disease_has_molecular_abnormality
- FANCG Gene Mutation [NCIt concept]
- Fanconi Anemia Complementation Group Gene Mutation [NCIt concept]
disease_mapped_to_gene
- FANCG Gene [NCIt concept]
disease_may_have_associated_disease
- Myelodysplastic Syndrome [NCIt concept]
pathogenesis_of_disease_involves_gene
- FANCG Gene [NCIt concept]
- FANCG wt Allele [NCIt concept]
related_to_genetic_biomarker
- FANCG Gene [NCIt concept]