AutoICD API

Q86.8

Billable

Oth congen malform syndromes due to known exogenous causes

Other congenital malformation syndromes due to known exogenous causes

Status

Billable / Specific

Parent Code

Q86

ICD-11 Mapping

1 equivalent

Coding Notes

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(3)
Q86.0

Fetal alcohol syndrome (dysmorphic)

BillableQ86.1

Fetal hydantoin syndrome

BillableQ86.2

Dysmorphism due to warfarin

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

LD2F.ZSyndromes with multiple structural anomalies, without predominant body system involvement, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(116)

SNOMED CT

UMLS

Clinical Terms

  • Fetal methylmercury syndrome
  • Foetal valproate spectrum disorder
  • Foetal iodine syndrome
  • Fetal misoprostol syndrome
  • Foetal misoprostol syndrome
  • Embryopathy caused by phenobarbital
  • Fetal methyl mercury syndrome
  • Indomethacin embryofetopathy
  • Foetal carbamazepine syndrome
  • Fetal disorder caused by anticonvulsant via placental transfer
  • Wiedemann's syndrome
  • Fetus affected by placental transfer of anticonvulsant
  • Embryofetopathy caused by methimazole
  • Thalidomide embryopathy syndrome
  • Fetal iodine syndrome
  • Fetal thalidomide syndrome
  • Foetal methyl mercury syndrome
  • Maternal phenylketonuria fetal effect
  • Foetal indomethacin syndrome
  • Phenobarbital embryopathy
  • Foetal anticonvulsant syndrome
  • Foetal thalidomide syndrome
  • Foetal benzodiazepine syndrome
  • Lenz's syndrome
  • Congenital malformation caused by valproic acid
  • Methimazole embryofetopathy
  • Fetal valproate spectrum disorder
  • Embryofetopathy caused by indomethacin
  • Congenital malformation caused by cytotoxic agents
  • Fetal toluene syndrome
  • Foetal toluene syndrome
  • Retinoid embryopathy
  • Embryopathy caused by isotretinoin
  • Embryopathy caused by mycophenolate mofetil
  • Multiple malformation syndrome due to non-infectious environmental agents
  • Fetal primidone syndrome
  • Narcotic embryopathy
  • Mycophenolate mofetil embryopathy
  • Fetal valproate syndrome
  • Foetal cocaine syndrome
  • Foetal primidone syndrome
  • Maternal phenylketonuria foetal effect
  • Fetal indomethacin syndrome
  • Fetal anticonvulsant syndrome
  • Fetal anomaly caused by antihypertensive drug
  • Fetal carbamazepine syndrome
  • Fetal cocaine syndrome
  • Foetal anomaly caused by antihypertensive drug
  • Fetal benzodiazepine syndrome
  • Foetal methylmercury syndrome
  • Isotretinoin syndrome
  • Maternal PKU fetal effect
  • Congenital malformation due to thalidomide
  • Foetal minoxidil syndrome
  • Embryopathy caused by retinoid
  • Foetus affected by placental transfer of anticonvulsant
  • Fetal minoxidil syndrome
Frequently Asked Questions
What is the ICD-10 code for oth congen malform syndromes due to known exogenous causes?

The ICD-10-CM code for oth congen malform syndromes due to known exogenous causes is Q86.8. The full clinical description is "Other congenital malformation syndromes due to known exogenous causes". Q86.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q86.8 mean?

ICD-10-CM code Q86.8 represents “Other congenital malformation syndromes due to known exogenous causes”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q86.8 a billable code?

Yes, Q86.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q86.8 in?

Q86.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q86.8 map to?

Q86.8 maps to 24 SNOMED CT concepts: 254246009, 878878007, 36193003, 715430001, 724144006, and 19 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q86.8?

Q86.8 is linked to 1 UMLS Concept Unique Identifier: C0478092. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q86.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like oth congen malform syndromes due to known exogenous causes affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q86.8?

Q86.8 maps to the ICD-11 code: LD2F.Z (Syndromes with multiple structural anomalies, without predominant body system involvement, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.