Coding Ahead

CasePilot

Medical Coding Assistant

Search and Code Lookup Tool

RedactPHI

HIPAA-Compliant PHI Redaction

DetectICD10CM

ICD-10-CM Code Detection

1 code page views remaining. Guest accounts are limited to 1 page view. Register free account to get 5 more views.

CPT® Code 0335U

Official Description

Rare diseases (constitutional/heritable disorders), whole genome sequence analysis, including small sequence changes, copy number variants, deletions, duplications, mobile element insertions, uniparental disomy (UPD), inversions, aneuploidy, mitochondrial genome sequence analysis with heteroplasmy and large deletions, short tandem repeat (STR) gene expansions, fetal sample, identification and categorization of genetic variants

Short Descr	RARE DS WHL GEN SEQ FETAL
Medium Descr	RARE DISEASES WHOLE GENOME SEQ ALYS FETAL SAMPLE
Long Descr	Rare diseases (constitutional/heritable disorders), whole genome sequence analysis, including small sequence changes, copy number variants, deletions, duplications, mobile element insertions, uniparental disomy (UPD), inversions, aneuploidy, mitochondrial genome sequence analysis with heteroplasmy and large deletions, short tandem repeat (STR) gene expansions, fetal sample, identification and categorization of genetic variants
CLIA Waived (QW)	No
APC Status Indicator	Service Paid under Fee Schedule or Payment System other than OPPS
Berenson-Eggers TOS (BETOS)	none
MUE	2