AutoICD API

Q92.8

Billable

Other specified trisomies and partial trisomies of autosomes

Other specified trisomies and partial trisomies of autosomes

Status

Billable / Specific

Parent Code

Q92

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Duplications identified by fluorescence in situ hybridization (FISH)
  • Duplications identified by in situ hybridization (ISH)
  • Duplications seen only at prometaphase

Includes

Conditions included under this code

  • unbalanced translocations and insertions

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(7)
Q92.0

Whole chromosome trisomy, nonmosaic (meiotic nondisjunction)

BillableQ92.1

Whole chromosome trisomy, mosaicism (mitotic nondisjunction)

BillableQ92.2

Partial trisomy

BillableQ92.5

Duplications with other complex rearrangements

BillableQ92.6

Marker chromosomes

Q92.7

Triploidy and polyploidy

BillableQ92.9

Trisomy and partial trisomy of autosomes, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

LD41.ZDuplications of the autosomes, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(376)

SNOMED CT

UMLS

Clinical Terms

  • MECP2 related disorder
  • Partial trisomy of chromosome 20
  • Duplication seen only at prometaphase (disorder)
  • Methyl-CpG (cytosine phosphate guanine) binding protein-2 disorder
  • Distal trisomy 19q
  • 14q11.2 microduplication syndrome
  • Duplications identified by in situ hybridization (ISH)
  • Proximal Xq28 duplication syndrome
  • Trisomy 17p13.3
  • 22q11.2 duplication syndrome
  • Partial trisomy of chromosome 10
  • Partial trisomy of chromosome 12
  • Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
  • Distal duplication 11q
  • Duplication of chromosome 10
  • Duplication of long arm of chromosome 5
  • Distal duplication 2q
  • Trisomy 17q11.2
  • Lubs X-linked intellectual disability syndrome
  • Partial trisomy of long arm of chromosome 1
  • Distal duplication 1p36
  • Duplication of chromosome 22
  • Distal trisomy 20q syndrome
  • 14q partial proximal trisomy syndrome
  • 4q partial trisomy syndrome
  • 19q partial trisomy syndrome
  • Partial trisomy of chromosome 14
  • Partial trisomy of chromosome 18
  • Schachenmann's syndrome
  • Syndactyly, nystagmus syndrome due to 2q31.1 microduplication
  • Duplication of chromosome 11
  • Trisomy 1q syndrome
  • Distal duplication 19q
  • 20q partial trisomy
  • Distal trisomy 6q
  • 10q partial trisomy syndrome
  • Distal trisomy 5q
  • Distal duplication 2p
  • Duplication of chromosome 5
  • Partial trisomy of chromosome 8
  • Methyl-CpG binding protein 2 related disorder
  • 11p15.4 microduplication syndrome
  • 8q partial trisomy syndrome
  • Distal trisomy 19q syndrome
  • Distal trisomy 11q
  • Complete trisomy 20 syndrome
  • 17q partial trisomy syndrome
  • Partial trisomy of long arm of chromosome 16
  • Distal duplication 20q
  • Mosaic trisomy chromosome 8
  • Partial trisomy of chromosome 11
  • Distal trisomy 4q
  • 15q11q13 microduplication syndrome
  • Telomeric duplication 2p
  • Trisomy 8q12
  • Complete trisomy 16 syndrome
  • Cat eye syndrome
  • Pseudotrisomy 18
  • Trisomy for short arm of chromosome 4
  • 3q26 microduplication syndrome
  • Trisomy 9
  • Trisomy 1q21.1
  • MECP2 (methyl-cytosine phosphate guanine binding protein-2) disorder
  • Partial trisomy of chromosome 3
  • Congenital nystagmus
  • Complete trisomy 9 syndrome
  • Duplication of chromosome 19
  • 20p partial trisomy syndrome
  • Partial trisomy of chromosome 4
  • Distal trisomy 1p36 syndrome
  • 4p partial trisomy syndrome
  • Duplications identified by fluorescence in situ hybridization (FISH)
  • 22q11.2 duplication
  • 5q35 microduplication syndrome
  • Partial trisomy of chromosome 5
  • Telomeric duplication 16q
  • Duplication seen only at prometaphase
  • Trisomy 10
  • Trisomy 8 mosaicism
  • Distal trisomy 16q
  • Chromosome 3q29 duplication syndrome
  • Distal trisomy 5q syndrome
  • 8q12 microduplication syndrome
  • Distal trisomy 7q11.23
  • 12p partial trisomy syndrome
  • Trisomy 6
  • Duplication of chromosome 7
  • Duplication of part of long arm of chromosome 16
  • Pendular nystagmus
  • Trisomy 3q29
  • Partial trisomy of chromosome 15
  • Duplication of chromosome 8
  • Partial duplication of long arm of chromosome 1
  • MECP2 duplication syndrome
  • 5p partial trisomy
  • Duplication of chromosome 12
  • Trisomy 10q22.3q23.3
  • Warkany syndrome
  • Chromosome 22q11.2 microduplication syndrome
  • Duplication of chromosome 2
  • Duplications seen only at prometaphase
  • 17p13.3 microduplication syndrome
  • Duplication of chromosome 6
  • Distal trisomy 20q
  • Methyl-CpG (cytosine phosphate guanine) binding protein-2 duplication syndrome
  • Duplication 1q
  • Trisomy 3q26
  • 1q21.1 microduplication syndrome
  • Distal trisomy 3p
  • Partial trisomy of short arm of chromosome 8
  • Partial trisomy of short arm of chromosome 1
  • Telomeric duplication 3p
  • Partial trisomy of chromosome 22
  • Telomeric duplication 1p36
  • Trisomy 4p syndrome
  • 14q partial trisomy
  • Partial trisomy of long arm of chromosome 5
  • Methyl-cytosine phosphate guanine binding protein-2 related disorder
  • 3p partial trisomy syndrome
  • Partial trisomy of chromosome 7
  • Distal trisomy 2q
  • Distal duplication 6q
  • Partial duplication short arm chromosome 8
  • Trisomy 8p syndrome
  • Partial trisomy of chromosome 16
  • Trisomy 11
  • Partial trisomy of chromosome 19
  • Syndactyly, nystagmus syndrome due to trisomy 2q31.1
  • Trisomy 7
  • Duplication of chromosome 4
  • Trisomy 15q11q13
  • 22q partial trisomy
  • Duplication 8p
  • Distal duplication 5q
  • 3q partial trisomy syndrome
  • CES - Cat eye syndrome
  • Mosaic trisomy 8 syndrome
  • 6q partial trisomy syndrome
  • Distal duplication 4q
  • Partial trisomy of chromosome 2
  • 3q29 microduplication
  • Duplication of chromosome 14
  • Duplication of chromosome 15
  • Distal 7q11.23 microduplication syndrome
  • Trisomy 11p15.4
  • Telomeric duplication 20q
  • 14q partial distal trisomy syndrome
  • 11q partial trisomy syndrome
  • Duplication of chromosome 20
  • 2p partial trisomy syndrome
  • Complete trisomy 22 syndrome
  • 10q22.3q23.3 microduplication syndrome
  • 7q partial trisomy
  • Telomeric duplication 11q
  • Complete trisomy 8 syndrome
  • Distal trisomy 2p
  • Distal duplication 16q
  • Duplication of chromosome 3
  • Trisomy 22
  • Distal duplication 3p
  • Trisomy 12
  • 18p partial trisomy syndrome
  • 2q partial trisomy syndrome
  • Distal trisomy 8q
  • Grisart Destree syndrome
  • Lubs X-linked mental retardation syndrome
  • Partial trisomy of chromosome 6
  • Duplication of short arm of chromosome 1
  • 17p partial trisomy syndrome
  • 17q11.2 microduplication syndrome
  • Trisomy 5q35
  • Mosaic trisomy 8
  • Duplication of chromosome 18
  • Distal trisomy 1p36
  • Trisomy 5p13
  • Trisomy 14q11.2
  • Trisomy 20p syndrome
  • Partial trisomy of short arm of chromosome 5
  • Trisomy 17p
  • Partial duplication of long arm of chromosome 15
  • Telomeric duplication 19q
  • 5p13 microduplication syndrome
  • Trisomy 8
  • 10p partial trisomy syndrome
  • Chromosome 22q11.2 duplication syndrome
  • Distal duplication 8q
  • Duplication of chromosome 16
Frequently Asked Questions
What is the ICD-10 code for other specified trisomies and partial trisomies of autosomes?

The ICD-10-CM code for other specified trisomies and partial trisomies of autosomes is Q92.8. The full clinical description is "Other specified trisomies and partial trisomies of autosomes". Q92.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q92.8 mean?

ICD-10-CM code Q92.8 represents “Other specified trisomies and partial trisomies of autosomes”. 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 Q92.8 a billable code?

Yes, Q92.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q92.8 in?

Q92.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q92.8?

Q92.8 has Excludes1 notes indicating codes that cannot be used together with it, including: trisomies of chromosomes 13, 18, 21 (Q90-Q91).

What SNOMED CT codes does Q92.8 map to?

Q92.8 maps to 98 SNOMED CT concepts: 48760005, 73035005, 782669004, 770794008, 4874006, and 93 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q92.8?

Q92.8 is linked to 4 UMLS Concept Unique Identifiers: C0432432, C2910365, C2910366, C0478098. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q92.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified trisomies and partial trisomies of autosomes 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 Q92.8?

Q92.8 maps to the ICD-11 code: LD41.Z (Duplications of the autosomes, 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.