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

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 -

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