Q87.19
BillableOther congen malform synd predom assoc with short stature
Other congenital malformation syndromes predominantly associated with short stature
Status
Billable / Specific
Parent Code
Q87.1Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Aarskog syndrome
- Cockayne syndrome
- De Lange syndrome
- Dubowitz syndrome
- Noonan syndrome
- Robinow-Silverman-Smith syndrome
- Russell-Silver syndrome
- Seckel syndrome
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
- 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
- Dwarfism-ichthyosiform erythroderma-mental deficiency syndrome2355008
- Rud syndrome2355008
- Rud's syndrome2355008
- Dubowitz syndrome2593002
- Dubowitz's syndrome2593002
- Congenital spherophakia4465002
- Spherophakia4465002
- Micrognathia-glossoptosis syndrome4602007
- Pierre Robin association4602007
- Pierre Robin syndrome4602007
- Robin sequence4602007
- Congenital bowing of tibia AND fibula9252005
- Congenital bowing of tibia and/or fibula9252005
- Neck webbing11731003
- Congenital webbing of neck11731003
- Webbed neck11731003
- Multiple malformation syndrome with senile-like appearance12674005
- Dandy-Walker deformity14447001
- Dandy-Walker malformation14447001
- Dandy-Walker syndrome14447001
- Aarskog syndrome14921002
- Russell's syndrome15069006
- Russell-Silver syndrome15069006
- Silver syndrome15069006
- Cockayne syndrome21086008
- Triangular skull28740008
- Trigonocephalia28740008
- Trigonocephalus28740008
- Trigonocephaly28740008
- Congenital small ears35045004
- Microtia35045004
- Congenital small lens35272001
- Microphakia35272001
- Amsterdam dwarf40354009
- Brachmann-de Lange syndrome40354009
- Bruck-de Lange syndrome40354009
- Cornelia de Lange syndrome40354009
- De Lange syndrome40354009
- Degenerative amstelodamensis typus40354009
- Degenerative amsterodamensis typus40354009
- Typus degenerativus amstelodamensis40354009
- Multiple malformation syndrome, small stature, without skeletal dysplasia41483000
- Angioma pigmentosum atrophicum44600005
- Atrophoderma pigmentosum44600005
- Kaposi dermatosis44600005
- Melanosis lenticularis progressiva44600005
- Pigmented epitheliomatosis44600005
- XP - Xeroderma pigmentosum44600005
- Xeroderma of Kaposi44600005
- Xeroderma pigmentosum44600005
- Bird-headed dwarf57917004
- Bird-headed dwarf of Seckel57917004
- Nanocephalic dwarf57917004
- Seckel syndrome57917004
- Congenital subaortic stenosis73660006
- Congenital subvalvular aortic stenosis73660006
- Acral dysostosis with facial and genital abnormalities76520005
- Fetal face syndrome76520005
- Foetal face syndrome76520005
- Robinow Silverman Smith syndrome76520005
- Robinow syndrome76520005
- Multiple malformation syndrome, moderate short stature, facial77701002
- Multiple malformation syndrome, moderate short stature, facial with or without genital features77701002
- Mulibrey nanism syndrome81604003
- Muscle, liver, brain, eye nanism syndrome81604003
- Perheentupa syndrome81604003
- Cleft mandible92822004
- Mandibular cleft92822004
- Congenital abnormal shape of frontal bone92912009
- Congenital misshapen frontal bone92912009
- Congenital abnormal shape of tibia92954007
- Congenital misshapen tibia92954007
- FAO - Fatty alcohol-nicotinamide adenine dinucleotide oxidase-reductase deficiency111303009
- Fatty alcohol-nicotinamide adenine dinucleotide oxidoreductase deficiency111303009
- Sjogren-Larsson syndrome111303009
- Sjögren-Larsson syndrome111303009
- Dentinogenesis imperfecta196286005
- Hereditary opalescent dentin196286005
- Ear, face and neck congenital anomalies204223000
- Atresia of posterior nares204508009
- Atresia of posterior naris204508009
- Choanal atresia204508009
- Congenital atresia of choana204508009
- Congenital atresia of posterior nares204508009
- Defect of vertebral segmentation205455005
- Congenital malformation syndromes associated with short stature205808005
- Noonan syndrome205824006
- Noonan's syndrome205824006
- Noonan-Ehmke syndrome205824006
- Turner-like syndrome205824006
- Chronic deafness232325008
- Bangstad syndrome237614004
- Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency237614004
- Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goitre, and primary gonadal insufficiency237614004
- Morbid obesity238136002
- Disturbance of hair cycle238734009
- Loose anagen hair syndrome238735005
- Dwarfism, alopecia, pseudoanodontia, cutis laxa239025003
- Cutaneous syndrome with ichthyosis239057002
- Hip pathological dislocation239759009
- Congenita hypotonic - sclerotic muscular dystrophy240062007
- Ullrich congenital muscular dystrophy240062007
- Congenital anomaly of angle of anterior chamber of eye251729009
- Congenital malformation of angle251729009
- Congenital malformation of angle of anterior chamber of eye251729009
- Goniodysgenesis251730004
- Osteodysplastic primordial dwarfism254101001
- Osteodysplastic primordial dwarfism, type 1254102008
- Congenital anomaly of anterior pituitary254255007
- Congenital malformation of anterior pituitary254255007
- Bent bone dysplasia group278832007
- Finger joint locking299110002
- Heritable disorder of neutrophil function402794002
- Developmental malformation of branchial arch402810002
- Amish brittle hair syndrome403796005
- BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome403796005
- BIDS syndrome403796005
- Brittle hair-impaired intellect-decreased fertility-short stature syndrome403796005
- Microspherophakia416671000
- Lentiglobus419281007
- Bowing deformity of lower leg609379005
- Warsaw breakage syndrome702829000
- KBG syndrome711156009
- Short stature, facial and skeletal anomalies, intellectual disability, macrodontia syndrome711156009
- Short stature-characteristic facies-mental retardation-macrodontia-skeletal anomalies syndrome711156009
- Gurrieri Sammito Bellussi syndrome715428003
- Skeletal dysplasia with epilepsy and short stature syndrome715428003
- Colobomatous microphthalmia715771008
- Microphthalmia with colobomatous cyst715771008
- Microphthalmos co-occurrent with congenital ocular coloboma715771008
- GMS syndrome716024001
- Goniodysgenesis with intellectual disability and short stature syndrome716024001
- Goniodysgenesis with mental deficiency and short stature716024001
- Haspeslagh Fryns Muelenaere syndrome716090004
- Short stature with craniofacial anomalies and genital hypoplasia syndrome716090004
- Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome716192009
- Thong Douglas Ferrante syndrome716192009
- Chitty Hall Baraitser syndrome716238003
- Deafness with epiphyseal dysplasia and short stature syndrome716238003
- Intellectual disability and short stature with hand contracture and genital anomaly syndrome716334004
- Prader Willi habitus with osteopenia and camptodactyly716334004
- Urban Rogers Meyer syndrome716334004
- Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome717914000
- Frydman Cohen Karmon syndrome717914000
- Atkin Flaitz syndrome718577005
- X-linked intellectual disability Atkin type718577005
- Mievis Verellen Dumoulin syndrome719213009
- Short stature Brussels type719213009
- Cleft palate with short stature and vertebral anomaly syndrome719466009
- Mathieu De Broca Bony syndrome719466009
- Absent thumb with short stature and immunodeficiency syndrome719685004
- Xeroderma pigmentosum and Cockayne syndrome complex719819004
- Oliver McFarlane syndrome719944006
- Trichomegaly with retina pigmentary degeneration and dwarfism syndrome719944006
- BOD (brachymorphism, onychodysplasia, dysphalangism) syndrome720573009
- Brachymorphism with onychodysplasia and dysphalangism syndrome720573009
- Senior syndrome720573009
- ACD (alopecia, contracture, dwarfism) mental retardation syndrome720979002
- ACD (alopecia, contracture, dwarfism) syndrome720979002
- Alopecia, contracture, dwarfism, intellectual disability syndrome720979002
- Short stature, pituitary and cerebellar defect and small sella turcica syndrome721072003
- Al Gazali Aziz Salem syndrome721073008
- Short stature with webbed neck and congenital heart disease syndrome721073008
- Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome721089006
- Macrocephaly, short stature, paraplegia syndrome722033000
- Volcke Soekarman syndrome722033000
- GEMSS (glaucoma, ectopia, microspherophakia, stiff joint, short stature) syndrome722450007
- GEMSS syndrome722450007
- Glaucoma, ectopia, microspherophakia, stiff joint, short stature syndrome722450007
- Cutaneous mastocytosis, short stature, hearing loss syndrome722453009
- Hennekam Beemer syndrome722453009
- Noonan syndrome-like disorder with loose anagen hair723444009
- Tosti syndrome723444009
- Trichothiodystrophy723551003
- Richieri Costa Pereira syndrome723998001
- Robin sequence with cleft mandible and limb anomalies syndrome723998001
- Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome723998001
- Deletion of part of chromosome 6726374009
- Deletion of part of long arm of chromosome 6726375005
- Eng Strom syndrome726734001
- Short stature locking fingers syndrome726734001
- Coxoauricular syndrome732248005
- Dysmorphism, short stature, deafness, disorder of sex development syndrome733050004
- Dysmorphism, short stature, deafness, pseudohermaphroditism syndrome733050004
- Say Meyer syndrome733066002
- Trigonocephaly, short stature, developmental delay syndrome733066002
- Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome733097003
- Passwell Goodman Siprkowski syndrome733097003
- Hypertrichosis, short stature, facial dysmorphism, developmental delay syndrome763618001
- Wiedemann Steiner syndrome763618001
- SHOX (short stature homeobox) related short stature763868006
- SHOX-related short stature763868006
- Short stature homeobox related short stature763868006
- Larsen-like osseous dysplasia, short stature syndrome764956007
- Dyssegmental dysplasia Silverman Handmaker type765204000
- X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome765471005
- Young Hughes syndrome765471005
- Severe lateral tibial bowing with short stature766819001
- Prader-Willi-like syndrome770680004
- X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome771148008
- X-linked colobomatous microphthalmia, microcephaly, short stature, psychomotor retardation syndrome771148008
- Char Douglas Dungan syndrome771179007
- Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome771179007
- Ataxia, photosensitivity, short stature syndrome773769008
- Fenton Wilkinson Toselano syndrome773769008
- Brachydactyly, short stature, retinitis pigmentosa syndrome782914000
- Onat syndrome783096008
- Subaortic stenosis and short stature syndrome783096008
- CBL (Cbl proto-oncogene) syndrome783143001
- Noonan syndrome-like disorder with juvenile myelomonocytic leukaemia783143001
- Noonan syndrome-like disorder with juvenile myelomonocytic leukemia783143001
- 15q26.3 microdeletion syndrome783551005
- Ichthyosis, short stature, brachydactyly, microspherophakia syndrome783551005
- Autosomal dominant Robinow syndrome890233009
- Autosomal recessive Robinow syndrome890237005
- Cockayne syndrome type 3890432001
- Cockayne syndrome type C890432001
- Classical Cockayne syndrome890433006
- Cockayne syndrome type 1890433006
- Cockayne syndrome type A890433006
- Cockayne syndrome type 2890434000
- Early onset Cockayne syndrome890434000
- 6q16 microdeletion syndrome1003380001
- Obesity due to 6q16 deletion1003380001
- Prader-Willi-like syndrome due to microdeletion 6q161003380001
- Congenital dysplasia of nail unit1142193008
- Congenital hypoplasia of adenohypophysis1144342008
- Congenital hypoplasia of anterior pituitary1144342008
- Aplasia of thumb1144446007
- SIM bHLH transcription factor 1-related Prader-Willi-like syndrome1229943004
- SIM1-related Prader-Willi-like syndrome1229943004
- MAGE family member L2-related Prader-Willi-like syndrome1229946007
- MAGEL2-related Prader-Willi-like syndrome1229946007
- Schaaf Yang syndrome1229946007
- Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome1281843005
- KMT2D-related choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome1281843005
- Lysine methyltransferase 2D-related choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome1281843005
- Liberfarb syndrome1284851009
- Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome1284851009
- BDV (Blakemore Durmaz Vasileiou) syndrome1340175001
- BDV syndrome1340175001
- Blakemore Durmaz Vasileiou syndrome1340175001
- CPE-related Prader-Willi-like syndrome1340175001
- Carboxypeptidase E-related Prader-Willi-like syndrome1340175001
- Genetic syndromic childhood obesity1359763002
- Anterior pituitary hormone deficiency2851000119101
UMLS
- AARSKOG SYNDROME, X-LINKEDC0175701
- AARSKOG-SCOTT SYNDROMEC0175701
- AASC0175701
- Aarskog DiseaseC0175701
- Aarskog SyndromeC0175701
- Aarskog syndromeC0175701
- Aarskog syndrome (disorder)C0175701
- Aarskog-Scott SyndromeC0175701
- Aarskog-Scott syndromeC0175701
- FACIODIGITOGENITAL SYNDROMEC0175701
- FACIOGENITAL DYSPLASIAC0175701
- FGDYC0175701
- Facio-Digito-Genital DysplasiaC0175701
- Facio-digito-genital dysplasiaC0175701
- Faciodigitogenital SyndromeC0175701
- Faciodigitogenital syndromeC0175701
- Faciogenital DysplasiaC0175701
- Faciogenital dysplasiaC0175701
- Scott Aarskog SyndromeC0175701
- aarskog syndromeC0175701
- aarskog's syndromeC0175701
- aarskog-scott syndromeC0175701
- aarskogs syndromeC0175701
- faciogenital dysplasiaC0175701
- greig syndromeC0175701
- greigs syndromeC0175701
- ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIESC0265205
- Acral Dysostosis with Facial and Genital AbnormalitiesC0265205
- Acral dysostosis with facial and genital abnormalitiesC0265205
- FETAL FACE SYNDROMEC0265205
- Fetal Face SyndromeC0265205
- Fetal face syndromeC0265205
- Foetal face syndromeC0265205
- Mesomelic Dwarfism-Small Genitalia SyndromeC0265205
- Mesomelic dwarfism-small genitalia syndromeC0265205
- ROBINOW DWARFISMC0265205
- Robinow DwarfismC0265205
- Robinow Silverman Smith syndromeC0265205
- Robinow SyndromeC0265205
- Robinow dwarfismC0265205
- Robinow syndromeC0265205
- Robinow syndrome (disorder)C0265205
- Robinow's syndromeC0265205
- Robinow-Silverman syndromeC0265205
- Robinow-Silverman-Smith SyndromeC0265205
- Robinow-Silverman-Smith syndromeC0265205
- fetal face syndromeC0265205
- robinow dwarfismC0265205
- robinow syndromeC0265205
- robinow's syndromeC0265205
- Amstelodamensis, Typus DegenerativusC0270972
- Amsterdam dwarfC0270972
- BDLSC0270972
- BRACHMANN-DE LANGE SYNDROMEC0270972
- Brachmann De Lange SyndromeC0270972
- Brachmann de Lange syndromeC0270972
- Brachmann-De Lange SyndromeC0270972
- Brachmann-de Lange syndromeC0270972
- Bruck-de Lange syndromeC0270972
- CDLC0270972
- CDLSC0270972
- CdLSC0270972
- Cornelia De Lange SyndromeC0270972
- Cornelia de Lange syndromeC0270972
- DE LANGE SYNDROMEC0270972
- DE LANGES SYNDROMEC0270972
- De Lange SyndromeC0270972
- De Lange syndromeC0270972
- De Lange syndrome (disorder)C0270972
- De Lange's SyndromeC0270972
- De Lange's syndromeC0270972
- Degenerative amstelodamensis typusC0270972
- Degenerative amsterodamensis typusC0270972
- Syndrome, Brachmann-De LangeC0270972
- TYPUS DEGENERATIVUS AMSTELODAMENSISC0270972
- Typus Degenerativus AmstelodamensisC0270972
- Typus degenerativus amstelodamensisC0270972
- brachmann de lange syndromeC0270972
- cornelia de lange syndromeC0270972
- cornelia de lange's syndromeC0270972
- cornelia de langes syndromeC0270972
- de Lange syndromeC0270972
- de lange syndromeC0270972
- lange syndrome cornelia deC0270972
- syndrome cornelia de langeC0270972
- Bird-Headed DwarfismC0265202
- Bird-headed dwarfC0265202
- Bird-headed dwarf of SeckelC0265202
- Microcephalic Primordial DwarfismC0265202
- Nanocephalic DwarfismC0265202
- Nanocephalic dwarfC0265202
- SCKLC0265202
- Seckel SyndromeC0265202
- Seckel syndromeC0265202
- Seckel syndrome (disorder)C0265202
- Seckel-Type DwarfismC0265202
- seckel bird head syndromeC0265202
- seckel syndromeC0265202
- seckel's syndromeC0265202
- seckels syndromeC0265202
- Cockayne SyndromeC0009207
- Cockayne syndromeC0009207
- Cockayne syndrome (disorder)C0009207
- Cockayne's syndromeC0009207
- Dwarfism-Retinal Atrophy-Deafness SyndromeC0009207
- Dwarfism-retinal atrophy-deafness syndromeC0009207
- Neill-Dingwall syndromeC0009207
- Progeria Like SyndromeC0009207
- Progeria-Like SyndromeC0009207
- Progeria-Like SyndromesC0009207
- Progeroid NanismC0009207
- Syndrome, CockayneC0009207
- Syndrome, Progeria-LikeC0009207
- cockayne syndromeC0009207
- cockayne's syndromeC0009207
- cockaynes syndromeC0009207
- mulvihill smith syndromeC0009207
- neill-dingwall syndromeC0009207
- progeroid syndromeC0009207
- syndrome cockayneC0009207
- DUBOWITZ SYNDROMEC0175691
- Dubowitz SyndromeC0175691
- Dubowitz syndromeC0175691
- Dubowitz's syndromeC0175691
- Dubowitz's syndrome (disorder)C0175691
- Dwarfism-eczema-peculiar facies syndromeC0175691
- Dwarfism, Silver RussellC0175693
- Dwarfism, Silver-RussellC0175693
- RSSC0175693
- RUSSELL-SILVER SYNDROMEC0175693
- Russell Silver SyndromeC0175693
- Russell's syndromeC0175693
- Russell-Silver DwarfismC0175693
- Russell-Silver SyndromeC0175693
- Russell-Silver SyndromesC0175693
- Russell-Silver syndromeC0175693
- Russell-Silver syndrome (disorder)C0175693
- SILVER-RUSSELL DWARFISMC0175693
- SRSC0175693
- Silver Russell DwarfismC0175693
- Silver Russell SyndromeC0175693
- Silver syndromeC0175693
- Silver-Russell DwarfismC0175693
- Silver-Russell SyndromeC0175693
- Silver-Russell dwarfismC0175693
- Silver-Russell syndromeC0175693
- Syndrome, Russell SilverC0175693
- Syndrome, Russell-SilverC0175693
- Syndrome, Silver-RussellC0175693
- Syndromes, Russell-SilverC0175693
- russell silver syndromeC0175693
- russell silvers syndromeC0175693
- russell syndromeC0175693
- russell's syndromeC0175693
- russell-silver syndromeC0175693
- silver russell syndromeC0175693
- silver syndromeC0175693
- silver-russell syndromeC0175693
- silvers syndromeC0175693
- Familial Turner SyndromeC0028326
- Familial Turner syndromeC0028326
- NOONAN SYNDROMEC0028326
- Noonan Ehmke SyndromeC0028326
- Noonan SyndromeC0028326
- Noonan syndromeC0028326
- Noonan's syndromeC0028326
- Noonan's syndrome (disorder)C0028326
- Noonan-Ehmke SyndromeC0028326
- Noonan-Ehmke syndromeC0028326
- Pseudo Ullrich Turner SyndromeC0028326
- Pseudo-Ullrich-Turner SyndromeC0028326
- Pseudo-Ullrich-Turner syndromeC0028326
- TURNER PHENOTYPE WITH NORMAL KARYOTYPEC0028326
- Turner Like SyndromeC0028326
- Turner Phenotype with Normal KaryotypeC0028326
- Turner Syndrome, FamilialC0028326
- Turner phenotype with normal karyotypeC0028326
- Turner phenotype, karyotype normalC0028326
- Turner's Phenotype, Karyotype NormalC0028326
- Turner's phenotype, karyotype normalC0028326
- Turner's phenotype, karyotype normal (disorder)C0028326
- Turner-Like SyndromeC0028326
- Turner-like syndromeC0028326
- Ullrich Noonan SyndromeC0028326
- Ullrich-Noonan SyndromeC0028326
- Ullrich-Noonan syndromeC0028326
- familial syndrome turnersC0028326
- male turner syndromeC0028326
- males syndrome turnersC0028326
- noonan syndromeC0028326
- noonan's syndromeC0028326
- noonans syndromeC0028326
- Other congen malform synd predom assoc with short statureC5140893
- Other congenital malformation syndromes predominantly associated with short statureC5140893
Frequently Asked Questions
What is ICD-10 code Q87.19?
ICD-10-CM code Q87.19 represents "Other congenital malformation syndromes predominantly associated with short stature". It is a billable/specific code that can be used on a claim.
Is Q87.19 a billable code?
Yes, Q87.19 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q87.19 in?
Q87.19 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q87.19?
Q87.19 has Excludes1 notes indicating codes that cannot be used together with it, including: Ellis-van Creveld syndrome (Q77.6); Smith-Lemli-Opitz syndrome (E78.72).
Are additional codes required with Q87.19?
Yes, when using Q87.19 you should also code: code(s) to identify all associated manifestations.
What SNOMED CT codes does Q87.19 map to?
Q87.19 maps to 118 SNOMED CT concepts: 11731003, 783551005, 1003380001, 720979002, 14921002, and 113 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q87.19?
Q87.19 is linked to 9 UMLS Concept Unique Identifiers: C0175701, C0265205, C0270972, C0265202, C0009207, and 4 more. 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.