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 |
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