Disease #00684 (SFM syndrome, somatic mosaic, OMIM:163200)

Official abbreviation -
Name SFM syndrome, somatic mosaic
OMIM ID 163200
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 3 genes HRAS, KRAS, NRAS
Associated tissues -
Disease features -
Remarks -

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