Billable / Specific Code
ICD-10-CM QA0.0141 is the diagnosis code for Syntaxin-binding protein 1-related disorder. This code falls under the section "Genetic disorders, not elsewhere classified" within Chapter 17 — Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0). It is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Medical coders and healthcare providers use this code to document and classify diagnoses in electronic health records, insurance claims, and clinical databases.
Understanding where QA0.0141 sits in the ICD-10-CM classification helps ensure proper coding:
Yes, QA0.0141 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
QA0.0141 is the ICD-10-CM diagnosis code for "Syntaxin-binding protein 1-related disorder". It is used by healthcare providers to classify and document this condition in medical records and insurance claims.
The parent code of QA0.0141 is QA0.014 ("Neurodevelopmental disorders, related to pathogenic variants in synapse related genes"). QA0.0141 provides a more specific classification within this category.
QA0.0141 is located in Section QA0 — "Genetic disorders, not elsewhere classified" within Chapter 17 of the ICD-10-CM Tabular List.
Use QA0.0141 when the patients documented diagnosis matches "Syntaxin-binding protein 1-related disorder" and the clinical documentation supports this level of specificity. Always verify with the latest ICD-10-CM guidelines and payer requirements.
The ICD-10-CM code for Syntaxin-binding protein 1-related disorder is QA0.0141.
Yes, QA0.0141 can be used as a primary diagnosis code since it is billable and specific.
QA0.0141 is in Chapter 17 of the ICD-10-CM Tabular List.
Yes, QA0.0141 is a valid ICD-10-CM code for the 2026 fiscal year, subject to official CMS updates.