AutoICD API

Q93.88

Billable

Other microdeletions

Other microdeletions

Status

Billable / Specific

Parent Code

Q93.8

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Miller-Dieker syndrome
  • Smith-Magenis syndrome

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

BillableQ93.89

Other deletions from the autosomes

Billable
Also Known As / Clinical Terms(591)

SNOMED CT

UMLS

Clinical Terms

  • Verheij syndrome
  • Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome
  • 1q21.1 contiguous gene deletion
  • Monosomy 20q13.33
  • Mesomelic dysplasia with acral synostoses Verloes David Pfeiffer type
  • Deletion of part of long arm of chromosome 5
  • 15q13.3 microdeletion
  • 6p22 microdeletion syndrome
  • Monosomy 2q23.1
  • SOX5 haploinsufficiency syndrome
  • Monosomy 1q41q42
  • SMS
  • HAFOUS - Hao Fountain syndrome
  • CHROMOSOME 17p13.3 DELETION SYNDROME
  • Distal monosomy 16p11.2
  • 2q24 microdeletion syndrome
  • Lissencephaly, Miller-Dieker
  • 1p partial monosomy
  • 20q11.2 microdeletion syndrome
  • Distal 17p13.1 microdeletion syndrome
  • Aldred syndrome
  • Monosomy 12q14
  • 2q32q33 microdeletion syndrome
  • 17q24.2 microdeletion syndrome
  • DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
  • 1q44 microdeletion syndrome
  • Deletion of part of chromosome 15
  • 12q14 microdeletion syndrome
  • Distal 17p13.3 microdeletion syndrome
  • Paternal 14q32.2 microdeletion
  • smith-magenis syndrome
  • 6q16 microdeletion syndrome
  • Chromosome microdeletion
  • Smith Magenis syndrome
  • 3q13 microdeletion syndrome
  • Monosomy 11q22.2q22.3
  • Mild intellectual development disorder
  • 1p31p32 microdeletion syndrome
  • 19p13.13 microdeletion syndrome
  • Microdeletion of chromosome 15q24
  • Distal 16p11.2 microdeletion syndrome
  • Speech delay
  • Prader-Willi-like syndrome due to microdeletion 6q16
  • 16p11.2p12.2 microdeletion syndrome
  • 14q22q23 microdeletion syndrome
  • Monosomy 12p12.1
  • Distal monosomy 17p13.3
  • Telomeric deletion 17p
  • magenis smith syndrome
  • 2q33.1 microdeletion syndrome
  • Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion
  • 10p12p11 microdeletion syndrome
  • Pseudo-Angelman syndrome
  • 14q12 microdeletion syndrome
  • Miller Dieker Syndrome
  • 10p partial monosomy syndrome
  • Deletion 10q22.3q23.3
  • lissencephaly syndrome
  • Monosomy 2p15p16.1
  • Monosomy 13q12.3
  • Chromosome 19p13.13 deletion syndrome
  • Lamb Shaffer syndrome
  • 12q15q21.1 microdeletion syndrome
  • Lissencephaly Syndrome, Miller-Dieker
  • 21q22.11q22.12 microdeletion syndrome
  • Distal 22q11.2 microdeletion syndrome
  • MDS
  • Lissencephaly due to 17p13.3 deletion
  • Cystinuria, type 1
  • Proximal 16p11.2 microdeletion syndrome
  • Type 1 lissencephaly
  • WAC-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome
  • 8q partial monosomy syndrome
  • 1q41-q42 microdeletion syndrome
  • Deletion of part of short arm of chromosome 16
  • 16p13.11 microduplication syndrome
  • 9q21.13 microdeletion syndrome
  • Deletion of part of chromosome 10
  • Dominant autosomal hereditary disorder, incomplete penetrance
  • Mild mental retardation, IQ in range 50-70
  • Monosomy 16p13.2
  • 9q partial monosomy syndrome
  • Classic lissencephaly
  • X-linked retinitis pigmentosa
  • Partial duplication of short arm of chromosome 16
  • Lissencephaly, Miller Dieker
  • Interstitial deletion of chromosome 15q24
  • Miller Dieker Lissencephaly Syndrome
  • Miller-Dieker lissencephaly syndrome
  • Monosomy 17q12
  • Monosomy 14q22q23
  • Severe neonatal hypotonia, seizures, encephalopathy syndrome due to 5q31.3 microdeletion
  • miller-dieker syndrome
  • Osteopoikilosis
  • Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
  • Verloes David syndrome
  • 3q subtelomere deletion syndrome
  • Deletion of part of long arm of chromosome 20
  • Partial deletion of long arm of chromosome 14
  • Paternal 20q13.2q13.3 microdeletion syndrome
  • 8q22.1 microdeletion syndrome
  • Monosomy 21q22.11q22.12
  • Obesity due to 6q16 deletion
  • WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome
  • Deletion of part of long arm of chromosome 3
  • WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome
  • 1q21.1 microdeletion
  • Partial deletion of long arm of chromosome 16
  • 5q31.3 microdeletion syndrome
  • Deletion of part of long arm of chromosome 16
  • Miller-Dieker Lissencephaly
  • Deletion of part of short arm of chromosome 6
  • Monosomy 9q31.1q31.3
  • 20q13.33 microdeletion syndrome
  • Deletion of long arm of chromosome 13
  • 20p12.3 microdeletion syndrome
  • 15q13.3 deletion syndrome
  • Buschke-Ollendorff syndrome
  • Hirschsprung disease and intellectual disability due to del(2)(q22)
  • Prader-Willi-like syndrome
  • Hirschsprung disease and intellectual disability due to 2q22 microdeletion
  • Microdeletion of chromosome 1q21.1
  • Monosomy 8p23.1
  • Cystinuria
  • Monosomy 1p31p32
  • 15q14 microdeletion syndrome
  • Deletion of part of chromosome 20
  • Deletion of part of long arm of chromosome 17
  • Deletion of part of short arm of chromosome 2
  • 15q11.2 microdeletion syndrome
  • Monosomy 10q22.3q23.3
  • Hirschsprung disease and intellectual disability due to monosomy 2q22
  • Monosomy 14q11.2
  • Monosomy 12q15q21.1
  • 15q24 deletion
  • 17q23.1q23.2 microdeletion syndrome
  • Monosomy 8q13
  • Partial deletion of long arm of chromosome 15
  • Deletion of part of short arm of chromosome 17
  • Monosomy 19p13.13
  • 10q partial monosomy
  • 7q31 microdeletion syndrome
  • Paternal monosomy 20q13.2q13.3
  • 22q partial monosomy
  • Hao Fountain syndrome
  • Monosomy 9q33.3q34.11
  • 9q31.1q31.3 microdeletion syndrome
  • Distal monosomy 7q
  • 12p12.1 microdeletion syndrome
  • 8p partial monosomy syndrome
  • 3q29 microdeletion syndrome
  • Monosomy 10p11.21p12.31
  • Deletion of part of long arm of chromosome 2
  • Distal monosomy 7q11.23
  • Deletion of part of short arm of chromosome 12
  • Xp22.3 microdeletion syndrome
  • Deletion of part of chromosome 17
  • 2q23.1 microdeletion syndrome
  • 15q24 microdeletion syndrome
  • Deletion of part of chromosome 13
  • Monosomy 15q11.2
  • Monosomy 1q44
  • Monosomy 20p12.3
  • Deletion of part of chromosome 19
  • Mild mental retardation (I.Q. 50-70)
  • Monosomy 6p22
  • Deletion of part of chromosome 11
  • 11q22.2q22.3 microdeletion syndrome
  • Monosomy 3q29
  • Deletion of part of chromosome 14
  • Monosomy 2q32q33
  • 1q41q42 microdeletion syndrome
  • 8q13 microdeletion syndrome
  • Monosomy 2q33.1
  • Deletion of part of long arm of chromosome 6
  • 1q21.1 microdeletion syndrome
  • 20p subtelomeric deletion syndrome
  • Hirschsprung disease-mental retardation syndrome
  • Recessive cystinuria
  • Nablus mask-like facial syndrome
  • Monosomy 21q22.13q22.2
  • 14q24.1q24.3 microdeletion syndrome
  • Partial trisomy of chromosome 16
  • Monosomy 17p13.3
  • Syndrome, Miller-Dieker
  • CHROMOSOME 17p11.2 DELETION SYNDROME
  • Deletion 9q33.3q34.11
  • Syndrome, Miller-Dieker Lissencephaly
  • Monosomy 14q12
  • Monosomy 14q24.1q24.3
  • Monosomy 16q24.1
  • 8q24.3 microdeletion syndrome
  • WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome
  • Hao Fountain syndrome due to 16p13.2 microdeletion
  • Monosomy 5q14.3
  • Monosomy 19p13.12
  • SATB2-associated syndrome
  • Deletion of part of short arm of chromosome 20
  • MDLS
  • DYRK1A syndrome
  • Partial deletion of the short arm of chromosome 1
  • 2p21 microdeletion syndrome
  • Monosomy 14q22-q23
  • Deletion of part of chromosome 5
  • Paternal monosomy 14q32.2
  • Mowat-Wilson syndrome due to 2q22 microdeletion
  • Deletion 10p11.21p12.31
  • 2p21 microdeletion syndrome without cystinuria
  • Chromosome 1q21.1 deletion syndrome
  • Mild intellectual disability
  • CSNU - Cystinuria
  • Smith-Magenis syndrome (disorder)
  • 9p13 microdeletion syndrome
  • Deletion of part of long arm of chromosome 12
  • 8p23.1 microdeletion syndrome
  • Mowat-Wilson syndrome due to del(2)q(22)
  • Lissencephaly Syndrome, Miller Dieker
  • Partial monosomy 17p
  • SATB2-associated syndrome due to chromosomal rearrangement
  • Monosomy 15q14
  • 7q partial monosomy
  • Deletion 8q24.3
  • Deletion 12q15q21.1
  • 14q22-q23 microdeletion syndrome
  • 5q14.3 microdeletion syndrome
  • Mesomelia synostoses syndrome Verloes David Pfeiffer type
  • Monosomy 1p35.2
  • Monosomy 8q24.3
  • Mowat-Wilson syndrome due to monosomy 2q22
  • 2p13.2 microdeletion syndrome
  • 21q partial proximal monosomy syndrome
  • 10q22.3q23.3 microdeletion syndrome
  • Monosomy 2q31.1
  • 17q12 microdeletion syndrome
  • Miller Dieker syndrome (disorder)
  • 1q partial monosomy
  • DYRK1A (dual specificity tyrosine phosphorylation regulated kinase 1A)-related intellectual disability syndrome
  • 15q24 microdeletion
  • 11q partial monosomy syndrome
  • Deletion of part of chromosome 22
  • DYRK1A-related intellectual disability syndrome
  • Monosomy 16p11.2p12.2
  • Duplication of part of short arm of chromosome 16
  • 13q12.3 microdeletion syndrome
  • Deletion of part of chromosome 21
  • 2p15p16.1 microdeletion syndrome
  • Trisomy 16p13.11
  • Monosomy 7q31
  • 16q24.1 microdeletion syndrome
  • Distal deletion of long arm of chromosome 7
  • 16p13.2 microdeletion syndrome
  • Monosomy 20p13
  • Special AT-rich sequence-binding protein 2-associated syndrome
  • Deletion of short arm of chromosome 19
  • 16p12.2 microdeletion syndrome
  • Monosomy 3q13
  • 14q11.2 microdeletion syndrome
  • Distal 7q11.23 microdeletion syndrome
  • Monosomy 9p13
  • Distal monosomy 22q11.2
  • 16p12.2 microdeletion
  • Partial deletion of chromosome 14q
  • 19p13.12 microdeletion syndrome
  • 9q33.3q34.11 microdeletion syndrome
  • Deletion of part of chromosome 6
  • 21q partial monosomy syndrome
  • 21q22.13q22.2 microdeletion syndrome
  • Hirschsprung disease-intellectual disability syndrome
  • Syndrome, Smith-Magenis
  • 2q31.1 microdeletion syndrome
  • Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
  • Mild mental retardation (Intelligence Quotient 50-70)
  • Chromosome Xp22.3 microdeletion syndrome
  • Monosomy 8q22.1
  • Microdeletion of chromosome 15q13.3
  • Monosomy 2q24
  • 1p35.2 microdeletion syndrome
  • Mowat-Wilson syndrome
  • Osteopoikilosis with short stature and intellectual disability syndrome
  • Slow to talk
  • magenis syndrome smith
  • Chromosome 17p deletion syndrome
  • Chromosome Xp11.3 microdeletion syndrome
  • 20p13 microdeletion syndrome
  • Duplication of chromosome 16
  • Monosomy 2p21
Frequently Asked Questions
What is the ICD-10 code for other microdeletions?

The ICD-10-CM code for other microdeletions is Q93.88. The full clinical description is "Other microdeletions". Q93.88 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q93.88 mean?

ICD-10-CM code Q93.88 represents “Other microdeletions”. 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 Q93.88 a billable code?

Yes, Q93.88 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q93.88 in?

Q93.88 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q93.88 map to?

Q93.88 maps to 133 SNOMED CT concepts: 6002006, 783061008, 16129004, 770401007, 4325000, and 128 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q93.88?

Q93.88 is linked to 3 UMLS Concept Unique Identifiers: C0795864, C0265219, C2910371. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q93.88 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other microdeletions 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 Q93.88?

There is no direct ICD-11 mapping available for Q93.88 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.