instruction
stringlengths
0
275
input
stringlengths
0
316
output
stringlengths
3
349
format
stringclasses
2 values
type
stringclasses
2 values
iteration
int64
1
5
__index_level_0__
int64
0
1.43M
A billing form lists Other oculocutaneous albinism as the primary diagnosis. What is the ICD-10-CM code?
The ICD-10-CM code for this diagnosis is E70328.
original
desc_to_code
1
3,600
Generate the ICD-10-CM code for this billing form.
The billing form lists Oculocutaneous albinism, unspecified.
E70329
original
desc_to_code
1
3,601
As a physician, clarify the ICD-10-CM code for this condition.
The patient has Chediak-Higashi syndrome.
The appropriate ICD-10-CM code is E70330.
original
desc_to_code
1
3,602
Map this clinical description to the correct ICD-10-CM code.
The patient has Hermansky-Pudlak syndrome.
The correct ICD-10-CM code is E70331.
original
desc_to_code
1
3,603
As a physician, provide the ICD-10-CM code for this diagnosis.
Other albinism with hematologic abnormality
The code is E70338.
original
desc_to_code
1
3,604
A billing form lists Albinism with hematologic abnormality, unspecified. What is the appropriate ICD-10-CM code?
The appropriate ICD-10-CM code is E70339.
original
desc_to_code
1
3,605
The patient's EHR excerpt shows Other specified albinism.
E7039
original
desc_to_code
1
3,606
Check if the ICD-10-CM code provided matches the clinical description.
The patient has Disorders of histidine metabolism, unspecified. Is the code E7040 accurate?
Yes, the code E7040 accurately reflects the clinical description.
original
desc_to_code
1
3,607
As a coding auditor, verify the ICD-10-CM code for this condition.
The patient was treated for Histidinemia.
The verified ICD-10-CM code is E7041.
original
desc_to_code
1
3,608
Choose the correct code for the ER case with this condition.
The ER case involves Other disorders of histidine metabolism.
The correct ICD-10-CM code for this ER case is E7049.
original
desc_to_code
1
3,609
Find the correct ICD-10-CM code for this condition.
The patient presents with Disorders of tryptophan metabolism.
The correct ICD-10-CM code is E705.
original
desc_to_code
1
3,610
Find the ICD-10-CM code for this condition.
The condition is Other disorders of aromatic amino-acid metabolism.
The ICD-10-CM code for this condition is E708.
original
desc_to_code
1
3,611
Generate the ICD-10-CM code for this billing scenario.
Disorder of aromatic amino-acid metabolism, unspecified
The billing code is E709.
original
desc_to_code
1
3,612
As a coder, generate the ICD-10-CM code for this billing form.
The form lists Maple-syrup-urine disease.
The ICD-10-CM code for this entry is E710.
original
desc_to_code
1
3,613
The patient's EHR indicates Isovaleric acidemia. What is the ICD-10-CM code?
The ICD-10-CM code for this condition is E71110.
original
desc_to_code
1
3,614
Map this clinical description to the appropriate ICD-10-CM code.
3-methylglutaconic aciduria
E71111
original
desc_to_code
1
3,615
Teach new coders how to code this condition.
The patient presents with Other branched-chain organic acidurias.
For this condition, new coders should use the code E71118.
original
desc_to_code
1
3,616
A patient's chart shows Methylmalonic acidemia. What is the ICD-10-CM code?
The appropriate code is E71120.
original
desc_to_code
1
3,617
Map this diagnosis to the correct ICD-10-CM code.
The patient has Propionic acidemia.
The correct code is E71121.
original
desc_to_code
1
3,618
Teach a new coder how to assign the ICD-10-CM code for this condition.
Other disorders of propionate metabolism
The correct code for Other disorders of propionate metabolism is E71128.
original
desc_to_code
1
3,619
Translate this clinical note into an ICD-10-CM code.
The note states Other disorders of branched-chain amino-acid metabolism.
The translated code is E7119.
original
desc_to_code
1
3,620
What is the correct code for this condition in a billing context?
The patient was diagnosed with Disorder of branched-chain amino-acid metabolism, unspecified.
The correct ICD-10-CM code for billing purposes is E712.
original
desc_to_code
1
3,621
As a coding auditor, clarify the ICD-10-CM code for this billing scenario.
The billing scenario involves Disorder of fatty-acid metabolism, unspecified.
The clarified code is E7130.
original
desc_to_code
1
3,622
Map the following clinical description to the appropriate ICD-10-CM code.
Long chain/very long chain acyl CoA dehydrogenase deficiency
E71310
original
desc_to_code
1
3,623
A billing form lists Medium chain acyl CoA dehydrogenase deficiency. What is the ICD-10-CM code?
The ICD-10-CM code is E71311.
original
desc_to_code
1
3,624
As an auditor, verify the ICD-10-CM code for this case in the billing form.
The billing form describes Short chain acyl CoA dehydrogenase deficiency.
The verified ICD-10-CM code is E71312.
original
desc_to_code
1
3,625
Find the ICD-10-CM code for this diagnosis.
The patient was treated for Glutaric aciduria type II.
E71313
original
desc_to_code
1
3,626
Tell me the ICD-10-CM code for this condition.
The patient has been experiencing Muscle carnitine palmitoyltransferase deficiency.
The ICD-10-CM code for this condition is E71314.
original
desc_to_code
1
3,627
What is the ICD-10-CM code for this condition?
The patient has Other disorders of fatty-acid oxidation.
The ICD-10-CM code is E71318.
original
desc_to_code
1
3,628
Generate the ICD-10-CM code for the following clinical description.
The patient presents with Disorders of ketone metabolism.
E7132
original
desc_to_code
1
3,629
Do you know the ICD-10-CM code for this patient's condition?
The patient has Other disorders of fatty-acid metabolism.
Yes, the correct code is E7139.
original
desc_to_code
1
3,630
As a physician, confirm the ICD-10-CM code for this condition.
The patient has Disorder of carnitine metabolism, unspecified.
The confirmed code is E7140.
original
desc_to_code
1
3,631
Find the ICD-10-CM code for this billing form entry.
The billing form lists Primary carnitine deficiency.
E7141
original
desc_to_code
1
3,632
Generate the ICD-10-CM code for this patient's diagnosis.
The diagnosis is Carnitine deficiency due to inborn errors of metabolism.
The generated code is E7142.
original
desc_to_code
1
3,633
Differentiate between possible ICD-10-CM codes for this condition.
The patient has Iatrogenic carnitine deficiency.
The most accurate code for this condition is E7143.
original
desc_to_code
1
3,634
A patient was admitted with Ruvalcaba-Myhre-Smith syndrome. What is the ICD-10-CM code?
E71440
original
desc_to_code
1
3,635
A patient's billing form lists Other secondary carnitine deficiency. What is the correct code?
E71448
original
desc_to_code
1
3,636
Check if the ICD-10-CM code matches the clinical description.
The patient's diagnosis is Peroxisomal disorder, unspecified. Is E7150 the correct code?
Yes, E7150 is the correct ICD-10-CM code for this diagnosis.
original
desc_to_code
1
3,637
Find the correct ICD-10-CM code for this condition.
The patient presents with Zellweger syndrome.
The correct ICD-10-CM code is E71510.
original
desc_to_code
1
3,638
What is the correct ICD-10-CM code for this billing form entry?
The billing form indicates Neonatal adrenoleukodystrophy.
The correct code is E71511.
original
desc_to_code
1
3,639
Do you know the ICD-10-CM code for this patient's condition in the EHR?
The patient's EHR indicates Other disorders of peroxisome biogenesis.
Yes, the code for this condition is E71518.
original
desc_to_code
1
3,640
As a physician, assign the ICD-10-CM code for this diagnosis.
The patient has Childhood cerebral X-linked adrenoleukodystrophy.
The ICD-10-CM code for this diagnosis is E71520.
original
desc_to_code
1
3,641
What is the correct code for this legal document?
The legal document mentions Adolescent X-linked adrenoleukodystrophy.
The correct code is E71521.
original
desc_to_code
1
3,642
As a student, find the ICD-10-CM code for this condition.
The patient was diagnosed with Adrenomyeloneuropathy.
E71522
original
desc_to_code
1
3,643
Choose the correct ICD-10-CM code for this ER case.
The ER report states Other X-linked adrenoleukodystrophy.
The correct code for this case is E71528.
original
desc_to_code
1
3,644
Do you know the ICD-10-CM code for this treatment plan?
Treatment plan: X-linked adrenoleukodystrophy, unspecified type
The ICD-10-CM code for X-linked adrenoleukodystrophy, unspecified type is E71529.
original
desc_to_code
1
3,645
Choose the correct ICD-10-CM code for this urgent care case.
The urgent care case involves Other group 2 peroxisomal disorders.
The correct code for this case is E7153.
original
desc_to_code
1
3,646
Differentiate possible codes for this condition among similar categories.
The patient was diagnosed with Rhizomelic chondrodysplasia punctata.
The correct ICD-10-CM code for this condition is E71540.
original
desc_to_code
1
3,647
Differentiate the possible ICD-10-CM codes for this condition.
The patient has Zellweger-like syndrome.
The correct ICD-10-CM code for Zellweger-like syndrome is E71541.
original
desc_to_code
1
3,648
Tell me the ICD-10-CM code for this referral note.
Referral note: Other group 3 peroxisomal disorders
E71542
original
desc_to_code
1
3,649
As a physician, confirm the ICD-10-CM code for this EHR excerpt.
The EHR excerpt shows Other peroxisomal disorders.
The confirmed code is E71548.
original
desc_to_code
1
3,650
Differentiate the possible ICD-10-CM codes for this condition.
The patient has Disorders of amino-acid transport, unspecified.
The correct ICD-10-CM code for this condition is E7200.
original
desc_to_code
1
3,651
Clarify the ICD-10-CM code for this EHR excerpt.
The EHR excerpt indicates Cystinuria.
The clarified ICD-10-CM code is E7201.
original
desc_to_code
1
3,652
Check if the ICD-10-CM code is accurate for this condition.
The patient has Hartnup's disease. Is E7202 correct?
Yes, E7202 is the correct ICD-10-CM code.
original
desc_to_code
1
3,653
Generate the ICD-10-CM code for this patient's condition.
The patient was diagnosed with Lowe's syndrome.
E7203
original
desc_to_code
1
3,654
Choose the correct ICD-10-CM code for this ER case.
The patient was treated for Cystinosis.
The correct ICD-10-CM code is E7204.
original
desc_to_code
1
3,655
Choose the correct ICD-10-CM code for this ER case.
The patient's condition is described as Other disorders of amino-acid transport.
The correct ICD-10-CM code for this ER case is E7209.
original
desc_to_code
1
3,656
Teach a new coder how to assign the ICD-10-CM code for this condition.
Disorders of sulfur-bearing amino-acid metabolism, unspecified
The correct code for Disorders of sulfur-bearing amino-acid metabolism, unspecified is E7210.
original
desc_to_code
1
3,657
A patient presents with Homocystinuria. What is the ICD-10-CM code?
E7211
original
desc_to_code
1
3,658
Check the ICD-10-CM code for this billing scenario.
The scenario involves Methylenetetrahydrofolate reductase deficiency.
The correct code is E7212.
original
desc_to_code
1
3,659
Check the accuracy of the ICD-10-CM code for this case.
The patient was treated for Other disorders of sulfur-bearing amino-acid metabolism.
The accurate code is E7219.
original
desc_to_code
1
3,660
Map this clinical description to the correct ICD-10-CM code.
The patient's symptoms include Disorder of urea cycle metabolism, unspecified.
The mapped ICD-10-CM code is E7220.
original
desc_to_code
1
3,661
Translate this clinical description into an ICD-10-CM code for insurance purposes.
Argininemia
E7221
original
desc_to_code
1
3,662
Verify the ICD-10-CM code for this patient's diagnosis.
The diagnosis is Arginosuccinic aciduria.
The verified code is E7222.
original
desc_to_code
1
3,663
For billing purposes, what is the ICD-10-CM code for this condition?
The condition is Citrullinemia.
The billing code is E7223.
original
desc_to_code
1
3,664
Teach a new coder how to assign the correct ICD-10-CM code for this condition.
The patient's diagnosis is Other disorders of urea cycle metabolism.
To code Other disorders of urea cycle metabolism, you should use E7229.
original
desc_to_code
1
3,665
As a medical student, how would you code this condition?
The patient has Disorders of lysine and hydroxylysine metabolism.
The appropriate ICD-10-CM code is E723.
original
desc_to_code
1
3,666
Do you know the ICD-10-CM code for this condition?
The patient's diagnosis is Disorders of ornithine metabolism.
Yes, the ICD-10-CM code for Disorders of ornithine metabolism is E724.
original
desc_to_code
1
3,667
As a student, find the ICD-10-CM code for this clinical scenario.
Disorder of glycine metabolism, unspecified
E7250
original
desc_to_code
1
3,668
Verify the accuracy of the ICD-10-CM code for this clinical scenario.
A patient has been diagnosed with Non-ketotic hyperglycinemia. Is the code E7251 correct?
Yes, the code E7251 is correct for this diagnosis.
original
desc_to_code
1
3,669
Generate the ICD-10-CM code for this diagnosis.
The patient has Trimethylaminuria.
E7252
original
desc_to_code
1
3,670
Find the ICD-10-CM code for this patient's condition.
The patient presents with Hyperoxaluria.
The code is E7253.
original
desc_to_code
1
3,671
Verify the ICD-10-CM code for the following clinical scenario.
A patient has been experiencing Other disorders of glycine metabolism.
The verified ICD-10-CM code is E7259.
original
desc_to_code
1
3,672
What is the ICD-10-CM code for this ER case?
The ER case involves Other specified disorders of amino-acid metabolism.
The ICD-10-CM code for this case is E728.
original
desc_to_code
1
3,673
A patient was admitted with Disorder of amino-acid metabolism, unspecified. What is the ICD-10-CM code?
The ICD-10-CM code for this admission is E729.
original
desc_to_code
1
3,674
Tell me the ICD-10-CM code for this medical record.
The medical record states Congenital lactase deficiency.
The ICD-10-CM code is E730.
original
desc_to_code
1
3,675
What is the correct code for this billing form entry?
Billing form indicates Secondary lactase deficiency.
The correct ICD-10-CM code for this entry is E731.
original
desc_to_code
1
3,676
Generate the ICD-10-CM code for this billing entry.
The billing form lists Other lactose intolerance.
E738
original
desc_to_code
1
3,677
Verify the ICD-10-CM code for this patient chart entry.
The entry states Lactose intolerance, unspecified.
The verified code is E739.
original
desc_to_code
1
3,678
Find the ICD-10-CM code for this patient's condition.
The patient has Glycogen storage disease, unspecified.
E7400
original
desc_to_code
1
3,679
What is the correct code for this clinical description in the billing form?
The billing form indicates von Gierke disease.
The correct ICD-10-CM code is E7401.
original
desc_to_code
1
3,680
As a medical coder, assign the ICD-10-CM code for this case.
The patient has Pompe disease.
The ICD-10-CM code for this case is E7402.
original
desc_to_code
1
3,681
Convert this clinical description into an ICD-10-CM code for insurance purposes.
The patient has Cori disease.
For insurance purposes, the code is E7403.
original
desc_to_code
1
3,682
For educational purposes, what is the ICD-10-CM code for this diagnosis?
The patient presents with McArdle disease.
The ICD-10-CM code for educational purposes is E7404.
original
desc_to_code
1
3,683
Choose the correct ICD-10-CM code for this ER case.
The ER report states Other glycogen storage disease.
The correct code for this case is E7409.
original
desc_to_code
1
3,684
As a physician, generate the ICD-10-CM code for this diagnosis.
The diagnosis is Disorder of fructose metabolism, unspecified.
The ICD-10-CM code is E7410.
original
desc_to_code
1
3,685
Explain to a new coder how to assign the ICD-10-CM code for this case.
The patient presents with Essential fructosuria.
For Essential fructosuria, use the code E7411.
original
desc_to_code
1
3,686
Check if the ICD-10-CM code matches the clinical description.
The patient was diagnosed with Hereditary fructose intolerance. The assigned code is E7412.
The code E7412 is correct for Hereditary fructose intolerance.
original
desc_to_code
1
3,687
Choose the correct ICD-10-CM code for this legal documentation.
The legal document states Other disorders of fructose metabolism.
The correct code for this case is E7419.
original
desc_to_code
1
3,688
Translate this clinical description into an ICD-10-CM code for billing purposes.
Disorders of galactose metabolism, unspecified
The billing code for this condition is E7420.
original
desc_to_code
1
3,689
Map this clinical description to the appropriate ICD-10-CM code.
A patient has been diagnosed with Galactosemia.
The appropriate ICD-10-CM code for this condition is E7421.
original
desc_to_code
1
3,690
A patient was treated for Other disorders of galactose metabolism. What is the ICD-10-CM code?
The ICD-10-CM code for this treatment is E7429.
original
desc_to_code
1
3,691
Verify the ICD-10-CM code for this legal documentation.
The legal document mentions Sucrase-isomaltase deficiency.
The correct code for legal purposes is E7431.
original
desc_to_code
1
3,692
Verify the ICD-10-CM code for this ER case.
The ER report states Other disorders of intestinal carbohydrate absorption.
The verified ICD-10-CM code is E7439.
original
desc_to_code
1
3,693
A patient's chart shows Disorders of pyruvate metabolism and gluconeogenesis. What is the correct code?
E744
original
desc_to_code
1
3,694
As a coder, ensure the ICD-10-CM code for Other specified disorders of carbohydrate metabolism is accurate.
Proposed code: E748
The code E748 is correct for Other specified disorders of carbohydrate metabolism.
original
desc_to_code
1
3,695
A patient presents with Disorder of carbohydrate metabolism, unspecified. What is the appropriate ICD-10-CM code for this condition?
The correct ICD-10-CM code for this condition is E749.
original
desc_to_code
1
3,696
Verify the ICD-10-CM code for this legal documentation.
The documentation states GM2 gangliosidosis, unspecified.
The verified code is E7500.
original
desc_to_code
1
3,697
Do you know the ICD-10-CM code for this diagnosis?
The patient was diagnosed with Sandhoff disease.
Yes, the correct code is E7501.
original
desc_to_code
1
3,698
What is the correct ICD-10-CM code for this patient's condition?
The condition is Tay-Sachs disease.
The correct code is E7502.
original
desc_to_code
1
3,699