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As a student, find the ICD-10-CM code for this clinical scenario.
Other GM2 gangliosidosis
E7509
original
desc_to_code
1
3,700
Verify the ICD-10-CM code for Unspecified gangliosidosis in this billing record.
Proposed code: E7510
The code E7510 is correct for Unspecified gangliosidosis.
original
desc_to_code
1
3,701
As a physician, generate the ICD-10-CM code for this diagnosis.
The patient has Mucolipidosis IV.
The appropriate code is E7511.
original
desc_to_code
1
3,702
Differentiate the possible ICD-10-CM codes for this condition.
The patient has Other gangliosidosis.
The most appropriate code for Other gangliosidosis is E7519.
original
desc_to_code
1
3,703
Differentiate possible codes for this insurance documentation.
The insurance documentation states Fabry (-Anderson) disease.
The correct code is E7521.
original
desc_to_code
1
3,704
As a medical coder, convert the following clinical description into an ICD-10-CM code.
The patient was diagnosed with Gaucher disease.
E7522
original
desc_to_code
1
3,705
Teach me how to code this condition using ICD-10-CM.
The patient was diagnosed with Krabbe disease.
For this condition, you would use the code E7523.
original
desc_to_code
1
3,706
Map this clinical description to the appropriate ICD-10-CM code for legal documentation.
The patient has Niemann-Pick disease type A.
The correct ICD-10-CM code for Niemann-Pick disease type A is E75240.
original
desc_to_code
1
3,707
As a physician, generate the ICD-10-CM code for this condition.
The patient's diagnosis is Niemann-Pick disease type B.
The code for this diagnosis is E75241.
original
desc_to_code
1
3,708
A patient was admitted with Niemann-Pick disease type C. What is the correct ICD-10-CM code?
E75242
original
desc_to_code
1
3,709
As a coding auditor, verify the ICD-10-CM code for this case.
The patient's chart indicates Niemann-Pick disease type D.
The verified code is E75243.
original
desc_to_code
1
3,710
Translate the following clinical description into the correct ICD-10-CM code.
The patient's diagnosis is Other Niemann-Pick disease.
E75248
original
desc_to_code
1
3,711
As a medical auditor, verify the ICD-10-CM code for this case.
The clinical notes state Niemann-Pick disease, unspecified.
The verified ICD-10-CM code is E75249.
original
desc_to_code
1
3,712
Convert the following clinical description into an ICD-10-CM code for insurance purposes.
Metachromatic leukodystrophy
The insurance code for Metachromatic leukodystrophy is E7525.
original
desc_to_code
1
3,713
Verify the ICD-10-CM code for the following clinical scenario.
A patient was admitted with Other sphingolipidosis.
After verification, the appropriate code is E7529.
original
desc_to_code
1
3,714
Do you know the ICD-10-CM code for this condition?
The patient has Sphingolipidosis, unspecified.
Yes, the ICD-10-CM code for this condition is E753.
original
desc_to_code
1
3,715
Teach new coders how to code this condition in an educational context.
The patient has Neuronal ceroid lipofuscinosis.
In an educational context, the code is E754.
original
desc_to_code
1
3,716
As a medical coder, convert this EHR excerpt into an ICD-10-CM code.
The EHR excerpt indicates Other lipid storage disorders.
The converted code is E755.
original
desc_to_code
1
3,717
As an auditor, verify the ICD-10-CM code for this case in the billing form.
The billing form describes Lipid storage disorder, unspecified.
The verified ICD-10-CM code is E756.
original
desc_to_code
1
3,718
For legal documentation, what is the ICD-10-CM code?
The legal document mentions Hurler's syndrome.
The legal code is E7601.
original
desc_to_code
1
3,719
Differentiate the possible ICD-10-CM codes for this condition.
The patient has Hurler-Scheie syndrome.
The correct ICD-10-CM code for Hurler-Scheie syndrome is E7602.
original
desc_to_code
1
3,720
As a medical coder, convert the following clinical description into an ICD-10-CM code.
The patient was diagnosed with Scheie's syndrome.
E7603
original
desc_to_code
1
3,721
For insurance documentation, what is the ICD-10-CM code for this condition?
The patient's diagnosis is Mucopolysaccharidosis, type II.
The insurance ICD-10-CM code is E761.
original
desc_to_code
1
3,722
Translate this clinical description into an ICD-10-CM code for educational purposes.
The patient has Morquio A mucopolysaccharidoses.
The educational code is E76210.
original
desc_to_code
1
3,723
As a physician, generate the ICD-10-CM code for this condition.
The patient has Morquio B mucopolysaccharidoses.
E76211
original
desc_to_code
1
3,724
For billing purposes, what is the ICD-10-CM code for this condition?
The patient was diagnosed with Morquio mucopolysaccharidoses, unspecified.
The billing code is E76219.
original
desc_to_code
1
3,725
Differentiate possible codes for this condition among similar categories.
The patient was diagnosed with Sanfilippo mucopolysaccharidoses.
The correct ICD-10-CM code for this condition is E7622.
original
desc_to_code
1
3,726
The physician noted Other mucopolysaccharidoses in the patient's record. What is the ICD-10-CM code?
E7629
original
desc_to_code
1
3,727
The clinical note states Mucopolysaccharidosis, unspecified.
E763
original
desc_to_code
1
3,728
Translate this clinical scenario into an ICD-10-CM code.
The scenario involves Other disorders of glucosaminoglycan metabolism.
The ICD-10-CM code for this scenario is E768.
original
desc_to_code
1
3,729
Verify the accuracy of the ICD-10-CM code for this clinical scenario.
A patient has been diagnosed with Glucosaminoglycan metabolism disorder, unspecified. Is the code E769 correct?
Yes, E769 is the correct ICD-10-CM code for Glucosaminoglycan metabolism disorder, unspecified.
original
desc_to_code
1
3,730
Choose the correct code for the ER case with this description.
The patient presents with Defects in post-translational modification of lysosomal enzymes.
The correct ICD-10-CM code for this ER case is E770.
original
desc_to_code
1
3,731
For consultation purposes, what is the ICD-10-CM code for this condition?
The patient presents with Defects in glycoprotein degradation.
The consultation ICD-10-CM code is E771.
original
desc_to_code
1
3,732
As a student, find the ICD-10-CM code for this clinical note.
The note states Other disorders of glycoprotein metabolism.
The code is E778.
original
desc_to_code
1
3,733
As a coder, map this description to the correct ICD-10-CM code.
Disorder of glycoprotein metabolism, unspecified
E779
original
desc_to_code
1
3,734
As an auditor, verify the ICD-10-CM code for this case.
The patient has Pure hypercholesterolemia, unspecified.
The verified code is E7800.
original
desc_to_code
1
3,735
Find the ICD-10-CM code for this condition in a legal documentation context.
The patient was treated for Familial hypercholesterolemia.
For legal documentation, use E7801.
original
desc_to_code
1
3,736
Map the following clinical description to the correct ICD-10-CM code.
A patient has Pure hyperglyceridemia.
The correct ICD-10-CM code is E781.
original
desc_to_code
1
3,737
Verify the ICD-10-CM code for this hospital discharge.
Hospital discharge: Mixed hyperlipidemia. Is E782 correct?
Yes, E782 is correct for Mixed hyperlipidemia.
original
desc_to_code
1
3,738
What is the ICD-10-CM code for this legal documentation entry?
The entry states Hyperchylomicronemia.
The code is E783.
original
desc_to_code
1
3,739
Differentiate between possible ICD-10-CM codes for this condition.
The patient has Other hyperlipidemia.
The most accurate code for Other hyperlipidemia is E784.
original
desc_to_code
1
3,740
Teach new coders how to code this condition.
A patient has been diagnosed with Hyperlipidemia, unspecified.
To code this condition, use the ICD-10-CM code E785.
original
desc_to_code
1
3,741
A patient was seen in the ER with Lipoprotein deficiency. What is the ICD-10-CM code?
The appropriate code for this ER case is E786.
original
desc_to_code
1
3,742
What is the ICD-10-CM code for Disorder of bile acid and cholesterol metabolism, unspecified in the context of legal documentation?
The ICD-10-CM code for this condition in legal documentation is E7870.
original
desc_to_code
1
3,743
What is the ICD-10-CM code for this billing scenario?
The patient was treated for Barth syndrome.
The ICD-10-CM code for billing is E7871.
original
desc_to_code
1
3,744
Verify the ICD-10-CM code for this hospital discharge.
Hospital discharge: Smith-Lemli-Opitz syndrome. Is E7872 correct?
Yes, E7872 is correct for Smith-Lemli-Opitz syndrome.
original
desc_to_code
1
3,745
The patient's discharge summary states Other disorders of bile acid and cholesterol metabolism.
E7879
original
desc_to_code
1
3,746
Differentiate the possible ICD-10-CM codes for this condition.
The patient has Lipoid dermatoarthritis.
The appropriate ICD-10-CM code for Lipoid dermatoarthritis is E7881.
original
desc_to_code
1
3,747
The EHR excerpt mentions Other lipoprotein metabolism disorders. What is the ICD-10-CM code?
E7889
original
desc_to_code
1
3,748
Differentiate possible ICD-10-CM codes for this legal documentation.
The legal document states Disorder of lipoprotein metabolism, unspecified.
The possible codes are E789 and E789.
original
desc_to_code
1
3,749
As an auditor, tell me the correct ICD-10-CM code for this case.
The clinical description is Hyperuricemia without signs of inflammatory arthritis and tophaceous disease.
The correct code is E790.
original
desc_to_code
1
3,750
Map the following clinical description to its ICD-10-CM code.
The description is Lesch-Nyhan syndrome.
The mapped code is E791.
original
desc_to_code
1
3,751
Teach new coders how to code this condition.
The patient has Myoadenylate deaminase deficiency.
To code this condition, use the ICD-10-CM code E792.
original
desc_to_code
1
3,752
As an auditor, confirm the ICD-10-CM code for this case.
The case involves Other disorders of purine and pyrimidine metabolism.
The confirmed code is E798.
original
desc_to_code
1
3,753
Verify the ICD-10-CM code for this legal documentation.
The legal document mentions Disorder of purine and pyrimidine metabolism, unspecified.
The correct code for legal purposes is E799.
original
desc_to_code
1
3,754
As an auditor, verify the ICD-10-CM code for this case.
The patient was treated for Hereditary erythropoietic porphyria. Is E800 accurate?
Yes, E800 is the accurate code for this case.
original
desc_to_code
1
3,755
As a physician, ensure the correct ICD-10-CM code is used for this diagnosis.
The patient's chart shows Porphyria cutanea tarda.
The correct code is E801.
original
desc_to_code
1
3,756
Generate the ICD-10-CM code for this patient's condition.
The patient was diagnosed with Unspecified porphyria.
E8020
original
desc_to_code
1
3,757
The billing form indicates Acute intermittent (hepatic) porphyria. What is the correct code?
The correct billing code is E8021.
original
desc_to_code
1
3,758
What is the correct code for this condition in a legal documentation context?
The patient was diagnosed with Other porphyria.
The correct ICD-10-CM code for legal documentation is E8029.
original
desc_to_code
1
3,759
As a medical coder, convert the following clinical description into the appropriate ICD-10-CM code.
The patient presents with Defects of catalase and peroxidase.
The correct ICD-10-CM code for this condition is E803.
original
desc_to_code
1
3,760
Teach a new coder how to map this clinical description to an ICD-10-CM code.
The patient has Gilbert syndrome.
For this condition, the correct ICD-10-CM code is E804.
original
desc_to_code
1
3,761
A coder needs to assign a code for Crigler-Najjar syndrome. What is the ICD-10-CM code?
E805
original
desc_to_code
1
3,762
Find the ICD-10-CM code for this patient's diagnosis.
The diagnosis is Other disorders of bilirubin metabolism.
E806
original
desc_to_code
1
3,763
A billing form lists Disorder of bilirubin metabolism, unspecified as the primary diagnosis. What is the ICD-10-CM code?
The ICD-10-CM code for this diagnosis is E807.
original
desc_to_code
1
3,764
As a physician, do you know the ICD-10-CM code for this condition?
The patient has Disorder of copper metabolism, unspecified.
Yes, the ICD-10-CM code is E8300.
original
desc_to_code
1
3,765
Clarify the ICD-10-CM code for this diagnosis.
The patient was diagnosed with Wilson's disease.
The ICD-10-CM code for this diagnosis is E8301.
original
desc_to_code
1
3,766
Translate this clinical impression into an ICD-10-CM code.
Clinical impression: Other disorders of copper metabolism
E8309
original
desc_to_code
1
3,767
As a physician, clarify the ICD-10-CM code for this condition.
The patient has Disorder of iron metabolism, unspecified.
The clarified ICD-10-CM code is E8310.
original
desc_to_code
1
3,768
Find the ICD-10-CM code for this EHR excerpt.
EHR notes state: Hereditary hemochromatosis.
E83110
original
desc_to_code
1
3,769
A coder needs to assign a code for Hemochromatosis due to repeated red blood cell transfusions. What is the ICD-10-CM code?
E83111
original
desc_to_code
1
3,770
What is the correct ICD-10-CM code for this condition?
The patient has Other hemochromatosis.
The correct ICD-10-CM code is E83118.
original
desc_to_code
1
3,771
Teach a new coder how to assign the ICD-10-CM code for this condition.
The patient has Hemochromatosis, unspecified.
The correct code for this condition is E83119.
original
desc_to_code
1
3,772
What is the correct ICD-10-CM code for this EHR excerpt?
The EHR excerpt indicates Other disorders of iron metabolism.
The correct code is E8319.
original
desc_to_code
1
3,773
A patient was diagnosed with Disorders of zinc metabolism. What is the ICD-10-CM code?
E832
original
desc_to_code
1
3,774
Map the clinical diagnosis Disorder of phosphorus metabolism, unspecified to its corresponding ICD-10-CM code.
E8330
original
desc_to_code
1
3,775
A student is learning to code Familial hypophosphatemia. What is the correct ICD-10-CM code?
The correct code for Familial hypophosphatemia is E8331.
original
desc_to_code
1
3,776
Teach a new coder how to assign the correct ICD-10-CM code for this condition.
Hereditary vitamin D-dependent rickets (type 1) (type 2)
To code Hereditary vitamin D-dependent rickets (type 1) (type 2), you should use E8332.
original
desc_to_code
1
3,777
As a physician, confirm the ICD-10-CM code for this billing form.
The billing form lists Other disorders of phosphorus metabolism.
The confirmed code is E8339.
original
desc_to_code
1
3,778
As a student, map the following condition to its ICD-10-CM code.
The patient has Disorders of magnesium metabolism, unspecified.
The mapped code is E8340.
original
desc_to_code
1
3,779
The physician documented Hypermagnesemia in the patient's record. What is the ICD-10-CM code?
E8341
original
desc_to_code
1
3,780
Convert the following clinical description into an ICD-10-CM code for insurance purposes.
Hypomagnesemia
The insurance code for Hypomagnesemia is E8342.
original
desc_to_code
1
3,781
Verify the accuracy of the ICD-10-CM code for this clinical scenario.
The patient's chart indicates Other disorders of magnesium metabolism.
The verified ICD-10-CM code is E8349.
original
desc_to_code
1
3,782
Clarify the ICD-10-CM code for this EHR excerpt.
The EHR excerpt describes Unspecified disorder of calcium metabolism.
The clarified ICD-10-CM code is E8350.
original
desc_to_code
1
3,783
During a routine check-up, the physician noted Hypocalcemia.
E8351
original
desc_to_code
1
3,784
A student is coding Hypercalcemia. What ICD-10-CM code should they assign?
They should assign E8352.
original
desc_to_code
1
3,785
As a coder, generate the ICD-10-CM code for this billing form.
The form lists Other disorders of calcium metabolism.
The ICD-10-CM code for this entry is E8359.
original
desc_to_code
1
3,786
Choose the correct code for the ER case with this description.
The ER case involves Hungry bone syndrome.
The correct ICD-10-CM code is E8381.
original
desc_to_code
1
3,787
Do you know the ICD-10-CM code for this condition?
Other disorders of mineral metabolism
Yes, the ICD-10-CM code for Other disorders of mineral metabolism is E8389.
original
desc_to_code
1
3,788
Translate the clinical description Disorder of mineral metabolism, unspecified into the corresponding ICD-10-CM code.
E839
original
desc_to_code
1
3,789
A billing form lists Cystic fibrosis with pulmonary manifestations. What is the ICD-10-CM code?
The ICD-10-CM code is E840.
original
desc_to_code
1
3,790
For billing purposes, what is the ICD-10-CM code for this diagnosis?
The patient has Meconium ileus in cystic fibrosis.
The ICD-10-CM code for billing purposes is E8411.
original
desc_to_code
1
3,791
Differentiate the possible ICD-10-CM codes for this condition.
The patient has Cystic fibrosis with other intestinal manifestations.
The most appropriate code for Cystic fibrosis with other intestinal manifestations is E8419.
original
desc_to_code
1
3,792
Find the ICD-10-CM code that best matches Cystic fibrosis with other manifestations.
The most accurate ICD-10-CM code for Cystic fibrosis with other manifestations is E848.
original
desc_to_code
1
3,793
Teach new coders how to code this condition.
The patient has Cystic fibrosis, unspecified.
To code this condition, use the ICD-10-CM code E849.
original
desc_to_code
1
3,794
As a physician, clarify the ICD-10-CM code for this diagnosis.
The patient has Non-neuropathic heredofamilial amyloidosis.
The appropriate code is E850.
original
desc_to_code
1
3,795
As a physician, clarify the ICD-10-CM code for this diagnosis.
The patient's chart shows Neuropathic heredofamilial amyloidosis.
The clarified code is E851.
original
desc_to_code
1
3,796
Differentiate the possible ICD-10-CM codes for this condition.
The patient has Heredofamilial amyloidosis, unspecified.
The appropriate code for this condition is E852.
original
desc_to_code
1
3,797
Find the ICD-10-CM code for this legal documentation.
The patient has Secondary systemic amyloidosis.
The ICD-10-CM code for this documentation is E853.
original
desc_to_code
1
3,798
Tell me the ICD-10-CM code for this clinical description.
The patient has been diagnosed with Organ-limited amyloidosis.
E854
original
desc_to_code
1
3,799