Index to Diseases and Injuries
Disorder › neurodevelopmental
Index code:F89
- CACNA1A-related QA0.0102
- DLG4-related synaptopathy QA0.0142
- FOXG1-related QA0.0151
- GRIN1-related QA0.011
- GRIN2A-related QA0.011
- GRIN2B-related QA0.011
- GRIN2D-related QA0.011
- GRIA1-related QA0.011
- GRIA2-related QA0.011
- GRIA3-related QA0.011
- GRIA4-related QA0.011
- GRIK2-related QA0.011
- other
- glutamate receptor, ionotropic, related QA0.011
- ion channel gene related QA0.0109
- receptor gene related QA0.012
- related to other genes associated with transcription and gene expression QA0.0159
- synapse related gene QA0.0149
- transporter or solute carrier gene related QA0.0139
- SCN2A-related QA0.0101
- SLC6A1-related QA0.0131
- STXBP1-related QA0.0141
- syntaxin-binding protein 1-related QA0.0141
- specified NEC F88
- related to pathogenic variants in specific genes NEC QA0.8
Use the index to find a code, then confirm it in the Tabular List before assigning it. A code ending in a dash is incomplete, and a code in [brackets] is a manifestation code reported after the underlying condition. Search the whole index.
Frequently asked questions
What is the ICD-10-CM code for Disorder › neurodevelopmental?
The ICD-10-CM Alphabetic Index directs "Disorder › neurodevelopmental" to F89. Subterms below it may lead to a more specific code. Always confirm the code in the Tabular List before assigning it.
ICD-10-CM Index to Diseases and Injuries maintained by CDC/NCHS (public domain), from the CMS FY2027 release.