759 Other and unspecified congenital anomalies (759.0-759.9) ICD-9-CM
The 759.0-759.9 block classified 759 other and unspecified congenital anomalies with 13 legacy diagnosis codes. None remain valid for claim submission; each code below links to its reference page with the official ICD-10-CM replacement under the CMS General Equivalence Mappings.
Retired Code Set
ICD-9-CM stopped being valid for U.S. claims with dates of service on or after October 1, 2015, when ICD-10-CM replaced it. Use this index for historical lookups and crosswalking; for current coding, start from the ICD-10-CM codes list or the ICD-9 / ICD-10 converter.
Legacy Codes in the 759.0-759.9 Block 13 codes
None of these codes remain valid for claim submission. Each code page shows its ICD-10-CM replacement under the CMS General Equivalence Mappings.
- 759.0 Anomalies of spleen
- 759.1 Adrenal gland anomaly
- 759.2 Endocrine anomaly NEC
- 759.3 Situs inversus
- 759.4 Conjoined twins
- 759.5 Tuberous sclerosis
- 759.6 Hamartoses NEC
- 759.7 Mult congen anomal NEC
- 759.81 Prader-willi syndrome
- 759.82 Marfan syndrome
- 759.83 Fragile x syndrome
- 759.89 Specfied cong anomal NEC
- 759.9 Congenital anomaly NOS
Questions About This Page
Are the 759.0-759.9 codes still billable?
No. Every code in this block became invalid for U.S. claims after September 30, 2015. Each code page linked above shows the ICD-10-CM replacement CMS assigned in the General Equivalence Mappings, and the ICD-9 / ICD-10 converter translates any of them directly.
What did the 759.0-759.9 block classify?
The block classified 759 other and unspecified congenital anomalies with 13 codes in the final ICD-9-CM release. It sat under Congenital anomalies (740–759) in the legacy hierarchy.
Related References
Source: final CMS ICD-9-CM release (version date October 1, 2014). Retired from U.S. claims after September 30, 2015.
