Disease #00070 (FANCD1 (Fanconi anemia, complementation group D1), OMIM:605724)

MVZ für Humangenetik Regensburg

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Official abbreviation	FANCD1
Name	Fanconi anemia, complementation group D1
OMIM ID	605724
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	BRCA2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-16 08:45:57 +00:00 (UTC)
Date last edited	N/A