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Fanconi Anemia Complementation Group A (MONDO:0009215)

Fanconi anemia caused by mutations of the FANCA gene. FANCA gene mutations are the most common cause of Fanconi anemia. This gene provides instructions for making a protein that is involved in the Fanconi anemia (FA) pathway.

Overview

Category

musculoskeletal system disorder

immune system disorder

hematologic disorder

Ontology ID

MONDO:0009215

Internal:10458

Synonyms

FANCA

FANCA Fanconi anaemia

FANCA Fanconi anemia

Fanconi Anemia, complementation group type a

Fanconi anaemia caused by mutation in FANCA

Fanconi anaemia complementation group type A

Fanconi anemia caused by mutation in FANCA

Fanconi anemia complementation group A

Fanconi anemia complementation group type A

Estren-Dameshek variant of Fanconi Anaemia

Estren-Dameshek variant of Fanconi Anemia

Estren-Dameshek variant of Fanconi pancytopenia

Fanconi Anaemia

Fanconi Anemia

Fanconi Anemia, Estren-Dameshek variant

Fanconi anemia, complementation group A

Mapped terms

DOID:0111095

GARD:0015170

GTR:AN1051558

MEDGEN:483333

NCIT:C125702

OMIM:227650

UMLS:C3469521

Child terms

Unknown children.

Results

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