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81441 - Inherited bone marrow failure syndromes (IBMFS) (eg, Fanconi anemia, dyskeratosis

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Procedure / ServiceInherited bone marrow failure syndromes (IBMFS) (eg, Fanconi anemia, dyskeratosis
Procedure / Service Description

Genetic and Molecular Testing Medical Necessity Guideline - BCS1L, C10orf2, COQ2, COX10, DGUOK, MPV17, OPA1, PDSS2, POLG, POLG2, RRM2B, SCO1, SCO2, SLC25A4, SUCLA2, SUCLG1, TAZ, TK2, and TYMP 81441 Inherited bone marrow failure syndromes (IBMFS) (eg, Fanconi anemia, dyskeratosis congenita, Diamond-Blackfan anemia, Shwachman-Diamond syndrome, GATA2 deficiency syndrome, congenital amegakaryocytic thrombocytopenia) sequence

Likely documents
  • Confirm benefit details
  • Submit clinical notes if requested by the plan
Next actions
  • Confirm the current plan policy before submission.
  • Use the insurer authorization workflow for this listed code.