Disease #06161 (OES (Oculoectodermal syndrome, somatic), OMIM:600268)

Official abbreviation OES
Name Oculoectodermal syndrome, somatic
OMIM ID 600268
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene KRAS
Associated tissues -
Disease features -
Remarks -

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