Q87.3
BillableCongenital malformation syndromes involving early overgrowth
Congenital malformation syndromes involving early overgrowth
Status
Billable / Specific
Parent Code
Q87Coding 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
- inborn errors of metabolism (E70-E88)
Use Additional Code
Additional codes that should follow this code
- code(s) to identify all associated manifestations
Also Known As / Clinical Terms
SNOMED CT
- Macrodactyly of toe4136000
- Macroencephaly9740002
- Megalencephaly9740002
- Amniocele18735004
- Congenital omphalocele18735004
- Omphalocele18735004
- Multiple malformation syndrome with early overgrowth48637007
- Weaver syndrome63119004
- Accelerated skeletal maturation, facial dysmorphism, failure to thrive syndrome73284007
- Marshall-Smith syndrome73284007
- Genetic giant80849007
- Giant80849007
- Giantism80849007
- Gigantism80849007
- Normal giant80849007
- Primordial giant80849007
- Beckwith's syndrome81780002
- Beckwith-Wiedemann syndrome81780002
- Exomphalos-macroglossia-gigantism syndrome81780002
- Wiedemann-Beckwith syndrome81780002
- Congenital overgrowth of foot205372002
- Parkes Weber syndrome234143003
- Congenital hypertrophy of tongue270516002
- Congenital macroglossia270516002
- Nephroblastoma302849000
- Wilm's tumor302849000
- Wilms tumor302849000
- Wilms tumour302849000
- Naevus flammeus416377005
- Nevus flammeus416377005
- PWS - Port-wine stain416377005
- Port wine stain of skin416377005
- Port-wine birthmark416377005
- Port-wine naevus416377005
- Port-wine nevus416377005
- Port-wine stain416377005
- Port-wine stain of skin416377005
- Portwine naevus416377005
- Portwine nevus416377005
- Bulldog syndrome439143004
- Simpson-Golabi-Behmel syndrome439143004
- Autosomal translocation709418005
- CLAPO (capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth) syndrome717765001
- CLAPO syndrome717765001
- Capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth syndrome717765001
- CLVM (capillary lymphatic venous malformation) with segmental distribution721105004
- Capillary, lymphatic, venous malformation with segmental distribution721105004
- KTS - Klippel Trenaunay syndrome721105004
- Klippel Trenaunay syndrome721105004
- Overgrowth, macrocephaly, facial dysmorphism syndrome722122000
- RNF135 (ring finger protein 135) related overgrowth syndrome722122000
- Ring finger protein 135 related overgrowth syndrome722122000
- Perlman syndrome722231005
- Angio-osteohypertrophic syndrome723991007
- Angioosteohypertrophic syndrome723991007
- Lipomatosis of subcutaneous tissue724852006
- Subcutaneous lipomatosis724852006
- Duplication of chromosome 15726354002
- Partial trisomy of chromosome 15726354002
- PIK3CA related overgrowth syndrome737037004
- PROS - phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha related overgrowth spectrum737037004
- Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha related overgrowth syndrome737037004
- Malan overgrowth syndrome763795006
- Sotos syndrome 2763795006
- DNA methyltransferase 3 alpha overgrowth syndrome768843007
- DNMT3A-related overgrowth syndrome768843007
- Tall stature, intellectual disability, facial dysmorphism syndrome768843007
- Tatton Brown Rahman overgrowth syndrome768843007
- Tatton Brown Rahman syndrome768843007
- Tall stature, scoliosis, macrodactyly of great toe syndrome770788000
- Tall stature, scoliosis, macrodactyly of hallux syndrome770788000
- HHML (hemihyperplasia multiple lipomatosis) syndrome771440006
- Hemihyperplasia with multiple lipomatosis syndrome771440006
- 15q overgrowth syndrome771477003
- Macrosomia, microphthalmia, cleft palate syndrome773282001
- Teebi Al Saleh Hassoon syndrome773282001
- GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumor) syndrome782722002
- GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumour) syndrome782722002
- GLOW syndrome782722002
- Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome782722002
- Global developmental delay, lung cysts, overgrowth, Wilms tumour syndrome782722002
- Segmental progressive overgrowth syndrome with fibroadipose hyperplasia787094005
- Partial duplication of long arm of chromosome 151162463004
- Tall stature, intellectual disability, renal anomalies syndrome1169359006
- Thauvin Robinet Faivre syndrome1169359006
- Overgrowth syndrome with 2q37 translocation1169362009
- Overgrowth, metaphyseal undermodeling, spondylar dysplasia syndrome1169363004
- Overgrowth, metaphyseal undermodelling, spondylar dysplasia syndrome1169363004
- Kosaki overgrowth syndrome1172898008
- Skeletal overgrowth, craniofacial dysmorphism, hyperelastic skin, white matter lesion syndrome1172898008
- Megalencephaly, severe kyphoscoliosis, overgrowth syndrome1260143005
- DCMO - diffuse capillary malformation with overgrowth1293116008
- Diffuse capillary malformation with overgrowth1293116008
- Luscan Lumish syndrome1300117002
- SET domain containing 2, histone lysine methyltransferase related overgrowth syndrome1300117002
- SETD2 (SET domain containing 2, histone lysine methyltransferase) related overgrowth syndrome1300117002
- SETD2-related overgrowth syndrome1300117002
- CHD8 overgrowth syndrome1304276001
- CHD8-related intellectual disability, autism, macrocephaly, tall stature syndrome1304276001
- Chromodomain helicase DNA binding protein 8 overgrowth syndrome1304276001
- Congenital umbilical hernia975231000000107
UMLS
- BECKWITH-WIEDEMANN SYNDROMEC0004903
- BWSC0004903
- Beckwith Wiedemann SyndromeC0004903
- Beckwith's syndromeC0004903
- Beckwith-Wiedemann SyndromeC0004903
- Beckwith-Wiedemann syndromeC0004903
- Beckwith-Wiedemann syndrome (disorder)C0004903
- EMG SYNDROMEC0004903
- EMG SyndromeC0004903
- EMG SyndromesC0004903
- EXOMPHALOS-MACROGLOSSIA-GIGANTISM SYNDROMEC0004903
- Exomphalos Macroglossia Gigantism SyndromeC0004903
- Exomphalos-Macroglossia-Gigantism SyndromeC0004903
- Exomphalos-Macroglossia-Gigantism SyndromesC0004903
- Exomphalos-macroglossia-gigantism syndromeC0004903
- Syndrome, Beckwith-WiedemannC0004903
- Syndrome, EMGC0004903
- Syndrome, Exomphalos-Macroglossia-GigantismC0004903
- Syndrome, WiedemannC0004903
- Syndrome, Wiedemann-BeckwithC0004903
- Syndrome, Wiedemann-Beckwith (WBS)C0004903
- WBSC0004903
- WIEDEMANN-BECKWITH SYNDROMEC0004903
- Wiedemann Beckwith SyndromeC0004903
- Wiedemann Beckwith Syndrome (WBS)C0004903
- Wiedemann SyndromeC0004903
- Wiedemann SyndromesC0004903
- Wiedemann-Beckwith SyndromeC0004903
- Wiedemann-Beckwith Syndrome (WBS)C0004903
- Wiedemann-Beckwith Syndromes (WBS)C0004903
- Wiedemann-Beckwith syndromeC0004903
- Wiedemann-Beckwith syndrome (WBS)C0004903
- beckwith syndromeC0004903
- beckwith syndrome wiedemannC0004903
- beckwith wiedemann syndromeC0004903
- beckwith's syndromeC0004903
- beckwith-wiedemann syndromeC0004903
- emg syndromeC0004903
- syndrome emgC0004903
- syndrome wiedemannC0004903
- wiedemann beckwith syndromeC0004903
- wiedemann syndromeC0004903
- CEREBRAL GIGANTISMC0175695
- CHROMOSOME 5q35 DELETION SYNDROMEC0175695
- Cerebral GigantismC0175695
- Cerebral GigantismsC0175695
- Cerebral giantC0175695
- Cerebral gigantismC0175695
- Cerebral gigantism syndromeC0175695
- Gigantism, CerebralC0175695
- Gigantisms, CerebralC0175695
- SOTOSC0175695
- SOTOS SYNDROMEC0175695
- SOTOS SYNDROME 1, FORMERLYC0175695
- SOTOS1, FORMERLYC0175695
- Sequence, SotosC0175695
- Soto SyndromeC0175695
- Soto's SyndromeC0175695
- Sotos SequenceC0175695
- Sotos SyndromeC0175695
- Sotos sequenceC0175695
- Sotos syndromeC0175695
- Sotos' SyndromeC0175695
- Sotos' syndromeC0175695
- Sotos' syndrome (disorder)C0175695
- Syndrome, SotosC0175695
- Syndrome, Sotos'C0175695
- cerebral gigantismC0175695
- soto syndromeC0175695
- sotos syndromeC0175695
- sotos' syndromeC0175695
- syndrome cerebral gigantismC0175695
- Camptodactyly-overgrowth-unusual faciesC0265210
- WEAVER SYNDROMEC0265210
- WEAVER-SMITH SYNDROMEC0265210
- WSSC0265210
- WVSC0265210
- Weaver Smith syndromeC0265210
- Weaver SyndromeC0265210
- Weaver syndromeC0265210
- Weaver syndrome (disorder)C0265210
- Weaver-Smith SyndromeC0265210
- Weaver-Smith syndromeC0265210
- syndrome weaverC0265210
- syndrome weaversC0265210
- weaver syndromeC0265210
- weaver's syndromeC0265210
- weaver-smith syndromeC0265210
- Congenital malformation syndromes involving early overgrowthC0495640
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 you should also code: 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.
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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.