AutoICD API

Q87.3

Billable

Congenital malformation syndromes involving early overgrowth

Congenital malformation syndromes involving early overgrowth

Status

Billable / Specific

Parent Code

Q87

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Beckwith-Wiedemann syndrome
  • Sotos syndrome
  • Weaver syndrome

Excludes 2

Conditions not included here, but the patient may have both

Use Additional Code

Additional codes that should follow this code

  • code(s) to identify all associated manifestations
Related Codes(6)
Q87.0

Congen malform syndromes predom affecting facial appearance

BillableQ87.1

Congenital malform syndromes predom assoc w short stature

Q87.2

Congenital malformation syndromes predom involving limbs

BillableQ87.4

Marfan syndrome

Q87.5

Oth congenital malformation syndromes w oth skeletal changes

BillableQ87.8

Oth congenital malformation syndromes, NEC

ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

LD2COvergrowth syndromesequivalentPrimary
Also Known As / Clinical Terms(344)

SNOMED CT

UMLS

Clinical Terms

  • KTS - Klippel Trenaunay syndrome
  • EXOMPHALOS-MACROGLOSSIA-GIGANTISM SYNDROME
  • PIK3CA related overgrowth syndrome
  • EMG Syndromes
  • GLOW syndrome
  • CLAPO syndrome
  • Cerebral gigantism
  • Hemihyperplasia with multiple lipomatosis syndrome
  • Angioosteohypertrophic syndrome
  • Exomphalos Macroglossia Gigantism Syndrome
  • Accelerated skeletal maturation, facial dysmorphism, failure to thrive syndrome
  • Weaver Smith syndrome
  • Sotos sequence
  • CHROMOSOME 5q35 DELETION SYNDROME
  • Kosaki overgrowth syndrome
  • RNF135 (ring finger protein 135) related overgrowth syndrome
  • Tall stature, intellectual disability, facial dysmorphism syndrome
  • Wiedemann Syndromes
  • CLAPO (capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth) syndrome
  • Portwine naevus
  • Beckwith Wiedemann Syndrome
  • Giantism
  • Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha related overgrowth syndrome
  • Exomphalos-Macroglossia-Gigantism Syndromes
  • Amniocele
  • Beckwith-Wiedemann Syndrome
  • WVS
  • Port-wine stain of skin
  • Subcutaneous lipomatosis
  • Congenital macroglossia
  • SOTOS
  • Ring finger protein 135 related overgrowth syndrome
  • weaver's syndrome
  • Cerebral Gigantisms
  • Congenital hypertrophy of tongue
  • wiedemann beckwith syndrome
  • Naevus flammeus
  • Sotos' Syndrome
  • Cerebral giant
  • DNMT3A-related overgrowth syndrome
  • Autosomal translocation
  • Wilms tumor
  • Syndrome, Wiedemann-Beckwith
  • WSS
  • Marshall-Smith syndrome
  • Giant
  • Malan overgrowth syndrome
  • Port-wine nevus
  • SET domain containing 2, histone lysine methyltransferase related overgrowth syndrome
  • Omphalocele
  • Syndrome, Beckwith-Wiedemann
  • beckwith syndrome wiedemann
  • Lipomatosis of subcutaneous tissue
  • Syndrome, Exomphalos-Macroglossia-Gigantism
  • Wiedemann Syndrome
  • Wiedemann-Beckwith Syndrome (WBS)
  • Port-wine naevus
  • Overgrowth, macrocephaly, facial dysmorphism syndrome
  • Sotos Syndrome
  • Weaver-Smith Syndrome
  • PROS - phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha related overgrowth spectrum
  • Congenital overgrowth of foot
  • Sotos syndrome 2
  • Port wine stain of skin
  • Soto's Syndrome
  • WBS
  • Diffuse capillary malformation with overgrowth
  • Luscan Lumish syndrome
  • Wilm's tumor
  • Wilms tumour
  • Partial trisomy of chromosome 15
  • Chromodomain helicase DNA binding protein 8 overgrowth syndrome
  • Simpson-Golabi-Behmel syndrome
  • Klippel Trenaunay syndrome
  • Overgrowth, metaphyseal undermodelling, spondylar dysplasia syndrome
  • Wiedemann-Beckwith syndrome
  • Portwine nevus
  • Camptodactyly-overgrowth-unusual facies
  • SOTOS SYNDROME 1, FORMERLY
  • syndrome cerebral gigantism
  • syndrome wiedemann
  • Bulldog syndrome
  • Thauvin Robinet Faivre syndrome
  • CHD8 overgrowth syndrome
  • Syndrome, Sotos'
  • Macrodactyly of toe
  • Tatton Brown Rahman syndrome
  • Weaver Syndrome
  • emg syndrome
  • SOTOS1, FORMERLY
  • Teebi Al Saleh Hassoon syndrome
  • DNA methyltransferase 3 alpha overgrowth syndrome
  • Overgrowth syndrome with 2q37 translocation
  • CHD8-related intellectual disability, autism, macrocephaly, tall stature syndrome
  • SETD2 (SET domain containing 2, histone lysine methyltransferase) related overgrowth syndrome
  • PWS - Port-wine stain
  • Global developmental delay, lung cysts, overgrowth, Wilms tumour syndrome
  • 15q overgrowth syndrome
  • Tatton Brown Rahman overgrowth syndrome
  • Weaver syndrome (disorder)
  • Beckwith's syndrome
  • Gigantism
  • Soto Syndrome
  • Angio-osteohypertrophic syndrome
  • Primordial giant
  • Tall stature, scoliosis, macrodactyly of great toe syndrome
  • Beckwith-Wiedemann syndrome (disorder)
  • Macroencephaly
  • Parkes Weber syndrome
  • Congenital umbilical hernia
  • Gigantisms, Cerebral
  • BWS
  • Syndrome, Sotos
  • Tall stature, scoliosis, macrodactyly of hallux syndrome
  • Gigantism, Cerebral
  • Capillary, lymphatic, venous malformation with segmental distribution
  • Perlman syndrome
  • beckwith syndrome
  • Duplication of chromosome 15
  • Skeletal overgrowth, craniofacial dysmorphism, hyperelastic skin, white matter lesion syndrome
  • syndrome weaver
  • Normal giant
  • Syndrome, EMG
  • Cerebral gigantism syndrome
  • Capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth syndrome
  • Sotos' syndrome (disorder)
  • syndrome emg
  • Syndrome, Wiedemann
  • Macrosomia, microphthalmia, cleft palate syndrome
  • Nephroblastoma
  • Tall stature, intellectual disability, renal anomalies syndrome
  • DCMO - diffuse capillary malformation with overgrowth
  • Port-wine stain
  • Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
  • syndrome weavers
  • Wiedemann-Beckwith Syndromes (WBS)
  • Wiedemann Beckwith Syndrome (WBS)
  • Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome
  • Multiple malformation syndrome with early overgrowth
  • Congenital omphalocele
  • Megalencephaly
  • Megalencephaly, severe kyphoscoliosis, overgrowth syndrome
  • Sequence, Sotos
  • HHML (hemihyperplasia multiple lipomatosis) syndrome
  • Syndrome, Wiedemann-Beckwith (WBS)
  • SETD2-related overgrowth syndrome
  • Partial duplication of long arm of chromosome 15
  • GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumor) syndrome
  • Nevus flammeus
  • Genetic giant
  • CLVM (capillary lymphatic venous malformation) with segmental distribution
  • GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumour) syndrome
  • Port-wine birthmark
  • Overgrowth, metaphyseal undermodeling, spondylar dysplasia syndrome
Frequently Asked Questions
What is the ICD-10 code for congenital malformation syndromes involving early overgrowth?

The ICD-10-CM code for congenital malformation syndromes involving early overgrowth is Q87.3. The full clinical description is "Congenital malformation syndromes involving early overgrowth". Q87.3 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q87.3 mean?

ICD-10-CM code Q87.3 represents “Congenital malformation syndromes involving early overgrowth”. 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 Q87.3 a billable code?

Yes, Q87.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q87.3 in?

Q87.3 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

Are additional codes required with Q87.3?

Yes, when using Q87.3, also report: code(s) to identify all associated manifestations.

What SNOMED CT codes does Q87.3 map to?

Q87.3 maps to 41 SNOMED CT concepts: 771477003, 73284007, 18735004, 723991007, 709418005, and 36 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q87.3?

Q87.3 is linked to 4 UMLS Concept Unique Identifiers: C0004903, C0175695, C0265210, C0495640. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q87.3 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation syndromes involving early overgrowth 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 Q87.3?

Q87.3 maps to the ICD-11 code: LD2C (Overgrowth syndromes).

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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.