CPT® Code Modifiers

-/+ Deleted, Replaced, Expanded Codes

section notes

Genetic Testing Code Modifiers

section notes

Dysmorphology

section notes
9M   FGFR1 (Pfeiffer and Kallman syndromes)
9N    FGFR2 (Crouzon, Jackson-Weiss, Apert, SaethreChotzen syndromes)
9O   FGFR3 (achondroplasia, hypochondroplasia, thanatophoric dysplasia, types I and II, Crouzon syndrome
9P   TWIST (Saethre-Chotzen syndrome)
9Q   DGCR, commonly called CATCH-22 (DiGeorge and 22q11 deletion syndromes)
9Z   Dysmorphology, not otherwise specified
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