Short answer · Medically reviewed summary · Last updated: 2023-07-10
Cystinuria is a rare genetic disorder that affects the kidneys, resulting in the formation of cystine stones in the urinary tract. The condition is characterized by the impaired reabsorption of the amino acid cystine in the kidneys, leading to its accumulation and subsequent stone formation.
1 people with Cystinuria have shared their first-person experience on this question at DiseaseMaps.
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ICD10 code of Cystinuria and ICD9 code
ICD-10 and ICD-9 codes for Cystinuria, with classification details for clinicians, coders and patients.
Cystinuria is a rare genetic disorder that affects the kidneys, resulting in the formation of cystine stones in the urinary tract. The condition is characterized by the impaired reabsorption of the amino acid cystine in the kidneys, leading to its accumulation and subsequent stone formation. To classify and identify medical conditions, healthcare professionals use a coding system known as the International Classification of Diseases (ICD).
In the ICD-10 coding system, the specific code for cystinuria is E72.01. This code falls under the broader category of "disorders of amino-acid transport and metabolism." The ICD-10 code provides a standardized way for healthcare providers to communicate and document the diagnosis of cystinuria, facilitating accurate and efficient medical record-keeping and billing processes.
In the previous coding system, ICD-9, cystinuria was classified under code 270.4. This code fell under the category of "disorders of amino acid transport and metabolism." However, it is important to note that the ICD-9 system is no longer in use, as it has been replaced by the more comprehensive ICD-10 coding system.
By utilizing specific codes like E72.01 for cystinuria, healthcare professionals can accurately identify and track the prevalence, treatment, and outcomes of this condition. This information can be valuable for research, public health planning, and ensuring appropriate care for individuals with cystinuria.
In the ICD-10 coding system, the specific code for cystinuria is E72.01. This code falls under the broader category of "disorders of amino-acid transport and metabolism." The ICD-10 code provides a standardized way for healthcare providers to communicate and document the diagnosis of cystinuria, facilitating accurate and efficient medical record-keeping and billing processes.
In the previous coding system, ICD-9, cystinuria was classified under code 270.4. This code fell under the category of "disorders of amino acid transport and metabolism." However, it is important to note that the ICD-9 system is no longer in use, as it has been replaced by the more comprehensive ICD-10 coding system.
By utilizing specific codes like E72.01 for cystinuria, healthcare professionals can accurately identify and track the prevalence, treatment, and outcomes of this condition. This information can be valuable for research, public health planning, and ensuring appropriate care for individuals with cystinuria.
Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2023-07-10
Medical disclaimer:
This information does not substitute professional medical advice. Always consult your doctor before making health decisions.
Source:
DiseaseMaps.org
The ICD10 for Cystinuria is E72.01
Posted Jul 14, 2018 by Teasley 2500
