Contents
1q31.3. Retinitis pigmentosa-12. 600105. Autosomal recessive. 3. CRB1. 604210. TEXT. A number sign (#) is used with this entry because of evidence that retinitis pigmentosa-12 (RP12) is caused by homozygous or compound heterozygous mutations in the CRB1 gene (604210) on chromosome 1q31.
FAQ icd 10 code for retinitis pigmentosa
What is the coding region for retinitis pigmentosa (RP11)?
No mutations in the coding region of the PRKCG gene in three families with retinitis pigmentosa linked to the RP11 locus on chromosome 19q. (Letter) Am. J. Hum. Genet. 65: 926-928, 1999.
How is retinitis pigmentosa (RP) characterized?
Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous group of retinal dystrophies characterized by a progressive degeneration of photoreceptors, eventually resulting in severe visual impairment. For a discussion of genetic heterogeneity of RP, see 268000.
What is the ICD 10 code for uveitis?
E11.319 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM E11.319 became effective on October 1, 2021. This is the American ICD-10-CM version of E11.319 – other international versions of ICD-10 E11.319 may differ.
What is the ICD 10 code for diabetic retinopathy?
Diabetic retinopathy associated with type ii diabetes mellitus. ICD-10-CM E11.319 is grouped within Diagnostic Related Group (s) (MS-DRG v38.0): 008 Simultaneous pancreas and kidney transplant. 010 Pancreas transplant.
ICD-10-CM Diabetic Retinopathy Coding Demonstration
Coding for Neoplasms, Endocrine and Z codes in ICD 10 CM
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