Disease #00123 (BMFS5 (BONE MARROW FAILURE SYNDROME 5), OMIM:618165)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	BMFS5
Name	BONE MARROW FAILURE SYNDROME 5
OMIM ID	618165
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TP53
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-16 10:13:54 +00:00 (UTC)
Date last edited	2023-06-16 10:22:30 +00:00 (UTC)