AutoICD API

Q93.89

Billable

Other deletions from the autosomes

Other deletions from the autosomes

Status

Billable / Specific

Parent Code

Q93.8

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

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

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(3)
Q93.81

Velo-cardio-facial syndrome

BillableQ93.82

Williams syndrome

BillableQ93.88

Other microdeletions

Billable
Also Known As / Clinical Terms(222)

SNOMED CT

UMLS

Clinical Terms

  • Chromosome 22 abnormalities with hypogammaglobulinemia
  • Deletion of part of long arm of chromosome 5
  • Distal monosomy 3p
  • 1p partial monosomy
  • 8p11.2 deletion syndrome
  • 13q minus syndrome
  • 16q24.3 microdeletion syndrome
  • 18q partial monosomy syndrome
  • Deletions seen only at prometaphase
  • Deletion of short arm of chromosome 18
  • Monosomy 22 syndrome
  • Neurofibromatosis type 1 microdeletion syndrome
  • 17q11 deletion syndrome
  • Distal monosomy 3p syndrome
  • Chromosome 4q deletion syndrome
  • Chromosome 3p deletion syndrome
  • 19q13.11 microdeletion syndrome
  • 1p36 deletion syndrome
  • 18p- syndrome
  • 18q minus syndrome
  • Multiple non-ossifying fibromatosis
  • 18p minus syndrome
  • Monosomy 16p13.11
  • Deletion seen only at prometaphase (disorder)
  • Familial polyposis coli
  • NF1 - Neurofibromatosis type 1
  • 3p25.3 deletion syndrome
  • Monosomy 8q21.11
  • 4q25 proximal deletion syndrome
  • 11p partial monosomy syndrome
  • 13q partial monosomy syndrome
  • 6q25 microdeletion syndrome
  • 8q partial monosomy syndrome
  • Deletion of part of short arm of chromosome 16
  • FAP - Familial adenomatous polyposis
  • Deletion of part of chromosome 10
  • 16p13.11 microdeletion syndrome
  • Chromosome 17q11.2 deletion syndrome
  • 8q21.11 microdeletion syndrome
  • Monosomy 16q24.3
  • 4q partial monosomy syndrome
  • Polyposis coli
  • Neurofibromatosis 1
  • Orbeli syndrome
  • Distal deletion 11q
  • Partial deletion of long arm of chromosome 16
  • Deletion of part of long arm of chromosome 16
  • Neurofibromatosis type 1
  • Deletion of long arm of chromosome 13
  • 1p21.3 microdeletion syndrome
  • Long arm 18 deletion syndrome
  • Deletion of part of long arm of chromosome 17
  • Deletion of long arm of chromosome 18
  • Proximal deletion of long arm of chromosome 18
  • Deletion of part of chromosome 18
  • 10q partial monosomy
  • Monosomy 1p21.3
  • 8p partial monosomy syndrome
  • Deletion of part of chromosome 17
  • Deletion of part of chromosome 13
  • Deletion of part of chromosome 19
  • Deletion of part of chromosome 11
  • FPC - Familial polyposis coli
  • Familial multiple polyposis syndrome
  • Deletion of part of long arm of chromosome 6
  • Neurofibromatosis, peripheral type
  • Familial adenomatous polyposis due to 5q22.2 microdeletion
  • Monosomy 6q25
  • Monosomy 1p36 syndrome
  • Distal monosomy 11q
  • Proximal monosomy 4q25
  • Adenomatous polyposis coli
  • 7p partial monosomy
  • 18p partial monosomy syndrome
  • Monosomy 17q11
  • Partial deletion of the short arm of chromosome 1
  • 3p syndrome
  • Deletions identified by fluorescence in situ hybridization (FISH)
  • Deletion of part of chromosome 5
  • Deletion of part of chromosome 4
  • Monosomy 22
  • Jacobsen syndrome
  • 4q21 microdeletion syndrome
  • Von Recklinghausen disease
  • Monosomy 4q21
  • Distal deletion of chromosome 13
  • Deletion 22
  • Monosomy 19q13.11
  • Familial adenomatous polyposis
  • 5q22.2 deletion syndrome
  • Complete monosomy of autosome
  • 1q partial monosomy
  • 11q partial monosomy syndrome
  • Distal 3p deletion
  • Chromosome 22 abnormalities with hypogammaglobulinaemia
  • Deletions identified by in situ hybridization (ISH)
  • Adenomatous polyposis
  • Deletion of long arm of chromosome 19
  • 3p partial monosomy syndrome
  • Deletion of part of chromosome 6
  • Distal monosomy 1p36
  • 18q- syndrome
  • Chromosome 1p36 deletion syndrome
  • 3p25.3 microdeletion syndrome
  • Proximal deletion of long arm of chromosome 4
  • Deletion seen only at prometaphase
  • Monosomy 8p11.2
  • Monosomy 22 and absence of immunoglobulin A
  • APC - Adenomatous polyposis coli
  • Distal partial deletion of long arm of chromosome 11
Frequently Asked Questions
What is the ICD-10 code for other deletions from the autosomes?

The ICD-10-CM code for other deletions from the autosomes is Q93.89. The full clinical description is "Other deletions from the autosomes". Q93.89 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q93.89 mean?

ICD-10-CM code Q93.89 represents “Other deletions from the 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 Q93.89 a billable code?

Yes, Q93.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q93.89 in?

Q93.89 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q93.89 map to?

Q93.89 maps to 57 SNOMED CT concepts: 16129004, 4135001, 4325000, 29257000, 719577000, and 52 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q93.89?

Q93.89 is linked to 4 UMLS Concept Unique Identifiers: C0432445, C2910372, C2910373, C0478100. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q93.89 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other deletions from the 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 Q93.89?

There is no direct ICD-11 mapping available for Q93.89 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.