Disease #00052 (FANCA (FANCONI ANEMIA, COMPLEMENTATION GROUP A), OMIM:227650)

Official abbreviation	FANCA
Name	FANCONI ANEMIA, COMPLEMENTATION GROUP A
OMIM ID	227650
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FANCA
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-03-03 15:58:40 +00:00 (UTC)
Date last edited	2023-06-16 09:10:23 +00:00 (UTC)

MVZ für Humangenetik Regensburg