AutoICD API

Q87.19

Billable

Other congen malform synd predom assoc with short stature

Other congenital malformation syndromes predominantly associated with short stature

Status

Billable / Specific

Parent Code

Q87.1

Coding 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

Use Additional Code

Additional codes that should follow this code

  • code(s) to identify all associated manifestations
Related Codes(1)
Q87.11

Prader-Willi syndrome

Billable
Also Known As / Clinical Terms(780)

SNOMED CT

UMLS

Clinical Terms

  • Rud's syndrome
  • Cutaneous syndrome with ichthyosis
  • Progeria-Like Syndromes
  • Degenerative amstelodamensis typus
  • Faciogenital dysplasia
  • BOD (brachymorphism, onychodysplasia, dysphalangism) syndrome
  • Ichthyosis, short stature, brachydactyly, microspherophakia syndrome
  • Pigmented epitheliomatosis
  • Cockayne syndrome (disorder)
  • brachmann de lange syndrome
  • Onat syndrome
  • progeroid syndrome
  • Dwarfism-Retinal Atrophy-Deafness Syndrome
  • GEMSS syndrome
  • Disturbance of hair cycle
  • Congenital bowing of tibia AND fibula
  • RSS
  • KMT2D-related choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome
  • Mulibrey nanism syndrome
  • Congenital malformation of angle of anterior chamber of eye
  • Cornelia de Lange syndrome
  • Congenital dysplasia of nail unit
  • cockayne's syndrome
  • Bird-headed dwarf
  • AARSKOG-SCOTT SYNDROME
  • Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome
  • Warsaw breakage syndrome
  • X-linked intellectual disability Atkin type
  • Cockayne syndrome type 1
  • GEMSS (glaucoma, ectopia, microspherophakia, stiff joint, short stature) syndrome
  • Hypertrichosis, short stature, facial dysmorphism, developmental delay syndrome
  • Brachymorphism with onychodysplasia and dysphalangism syndrome
  • Gurrieri Sammito Bellussi syndrome
  • robinow dwarfism
  • Silver Russell Syndrome
  • Bowing deformity of lower leg
  • Ullrich Noonan Syndrome
  • Microcephalic Primordial Dwarfism
  • Obesity due to 6q16 deletion
  • Mesomelic Dwarfism-Small Genitalia Syndrome
  • Short stature, pituitary and cerebellar defect and small sella turcica syndrome
  • Congenital subaortic stenosis
  • Robinow Syndrome
  • Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome
  • Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
  • BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome
  • SIM bHLH transcription factor 1-related Prader-Willi-like syndrome
  • Congenita hypotonic - sclerotic muscular dystrophy
  • Say Meyer syndrome
  • Atresia of posterior naris
  • Brittle hair-impaired intellect-decreased fertility-short stature syndrome
  • Xeroderma pigmentosum and Cockayne syndrome complex
  • Scott Aarskog Syndrome
  • Noonan's syndrome (disorder)
  • CdLS
  • Deletion of part of long arm of chromosome 6
  • CPE-related Prader-Willi-like syndrome
  • NOONAN SYNDROME
  • Colobomatous microphthalmia
  • Congenital anomaly of angle of anterior chamber of eye
  • Rud syndrome
  • De Lange's Syndrome
  • SCKL
  • Dandy-Walker deformity
  • TYPUS DEGENERATIVUS AMSTELODAMENSIS
  • Facio-Digito-Genital Dysplasia
  • seckel bird head syndrome
  • Autosomal dominant Robinow syndrome
  • Seckel syndrome (disorder)
  • Syndrome, Russell-Silver
  • syndrome cockayne
  • CBL (Cbl proto-oncogene) syndrome
  • Liberfarb syndrome
  • Robinow-Silverman-Smith Syndrome
  • Silver-Russell dwarfism
  • Coxoauricular syndrome
  • Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency
  • De Lange Syndrome
  • russell silvers syndrome
  • russell-silver syndrome
  • Xeroderma pigmentosum
  • CDL
  • Short stature locking fingers syndrome
  • Thong Douglas Ferrante syndrome
  • Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goitre, and primary gonadal insufficiency
  • Russell-Silver Syndromes
  • Dubowitz's syndrome
  • Congenital small ears
  • GMS syndrome
  • Cleft mandible
  • Silver syndrome
  • DUBOWITZ SYNDROME
  • robinow's syndrome
  • Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome
  • DE LANGES SYNDROME
  • FGDY
  • Hennekam Beemer syndrome
  • Fetal Face Syndrome
  • Perheentupa syndrome
  • Urban Rogers Meyer syndrome
  • Trigonocephaly, short stature, developmental delay syndrome
  • Sjogren-Larsson syndrome
  • greigs syndrome
  • Syndrome, Cockayne
  • Dyssegmental dysplasia Silverman Handmaker type
  • Sjögren-Larsson syndrome
  • Fatty alcohol-nicotinamide adenine dinucleotide oxidoreductase deficiency
  • Wiedemann Steiner syndrome
  • cornelia de lange's syndrome
  • MAGE family member L2-related Prader-Willi-like syndrome
  • Syndromes, Russell-Silver
  • Multiple malformation syndrome, moderate short stature, facial with or without genital features
  • X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome
  • Skeletal dysplasia with epilepsy and short stature syndrome
  • Frydman Cohen Karmon syndrome
  • Morbid obesity
  • X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome
  • Turner-Like Syndrome
  • Choanal atresia
  • Turner's phenotype, karyotype normal
  • Amsterdam dwarf
  • SHOX (short stature homeobox) related short stature
  • Trigonocephalia
  • Glaucoma, ectopia, microspherophakia, stiff joint, short stature syndrome
  • Nanocephalic Dwarfism
  • Congenital malformation of angle
  • Silver-Russell Syndrome
  • Microspherophakia
  • Chitty Hall Baraitser syndrome
  • Robin sequence with cleft mandible and limb anomalies syndrome
  • Neill-Dingwall syndrome
  • TURNER PHENOTYPE WITH NORMAL KARYOTYPE
  • Dysmorphism, short stature, deafness, disorder of sex development syndrome
  • Congenital atresia of posterior nares
  • Cockayne syndrome type C
  • Noonan syndrome-like disorder with juvenile myelomonocytic leukaemia
  • Senior syndrome
  • FACIODIGITOGENITAL SYNDROME
  • 15q26.3 microdeletion syndrome
  • Congenital subvalvular aortic stenosis
  • Dwarfism, Silver Russell
  • Dandy-Walker malformation
  • BRACHMANN-DE LANGE SYNDROME
  • Pseudo-Ullrich-Turner Syndrome
  • Progeroid Nanism
  • Early onset Cockayne syndrome
  • Dubowitz's syndrome (disorder)
  • Robinow syndrome (disorder)
  • Turner's phenotype, karyotype normal (disorder)
  • Triangular skull
  • Osteodysplastic primordial dwarfism
  • ACD (alopecia, contracture, dwarfism) syndrome
  • Melanosis lenticularis progressiva
  • Goniodysgenesis
  • male turner syndrome
  • KBG syndrome
  • Ullrich-Noonan Syndrome
  • Bird-Headed Dwarfism
  • Cockayne Syndrome
  • russell's syndrome
  • Goniodysgenesis with intellectual disability and short stature syndrome
  • Webbed neck
  • Turner Like Syndrome
  • Atkin Flaitz syndrome
  • Osteodysplastic primordial dwarfism, type 1
  • Muscle, liver, brain, eye nanism syndrome
  • BDV (Blakemore Durmaz Vasileiou) syndrome
  • Subaortic stenosis and short stature syndrome
  • Progeria Like Syndrome
  • Eng Strom syndrome
  • Prader Willi habitus with osteopenia and camptodactyly
  • Dandy-Walker syndrome
  • Aarskog Disease
  • Short stature-characteristic facies-mental retardation-macrodontia-skeletal anomalies syndrome
  • Congenital malformation of anterior pituitary
  • Congenital hypoplasia of adenohypophysis
  • Loose anagen hair syndrome
  • Ear, face and neck congenital anomalies
  • Haspeslagh Fryns Muelenaere syndrome
  • seckels syndrome
  • Amstelodamensis, Typus Degenerativus
  • Ullrich congenital muscular dystrophy
  • Syndrome, Silver-Russell
  • Progeria-Like Syndrome
  • Silver Russell Dwarfism
  • Severe lateral tibial bowing with short stature
  • Bird-headed dwarf of Seckel
  • Congenital anomaly of anterior pituitary
  • Congenital misshapen frontal bone
  • Foetal face syndrome
  • Fenton Wilkinson Toselano syndrome
  • Multiple malformation syndrome, small stature, without skeletal dysplasia
  • Cleft palate with short stature and vertebral anomaly syndrome
  • Passwell Goodman Siprkowski syndrome
  • Robinow-Silverman syndrome
  • Syndrome, Brachmann-De Lange
  • aarskog's syndrome
  • Turner Syndrome, Familial
  • Developmental malformation of branchial arch
  • Dwarfism, alopecia, pseudoanodontia, cutis laxa
  • Al Gazali Aziz Salem syndrome
  • Noonan's syndrome
  • Cockayne syndrome type 2
  • Congenital webbing of neck
  • Neck webbing
  • Aarskog Syndrome
  • Finger joint locking
  • Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome
  • Congenital hypoplasia of anterior pituitary
  • males syndrome turners
  • Young Hughes syndrome
  • Macrocephaly, short stature, paraplegia syndrome
  • Mathieu De Broca Bony syndrome
  • cockaynes syndrome
  • Short stature, facial and skeletal anomalies, intellectual disability, macrodontia syndrome
  • Familial Turner Syndrome
  • AAS
  • Cockayne syndrome type A
  • Short stature homeobox related short stature
  • Lentiglobus
  • Anterior pituitary hormone deficiency
  • Microtia
  • Char Douglas Dungan syndrome
  • XP - Xeroderma pigmentosum
  • Russell-Silver Dwarfism
  • Bangstad syndrome
  • SIM1-related Prader-Willi-like syndrome
  • Kaposi dermatosis
  • Aarskog syndrome (disorder)
  • Dentinogenesis imperfecta
  • Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome
  • Acral dysostosis with facial and genital abnormalities
  • Trichothiodystrophy
  • Aplasia of thumb
  • Ataxia, photosensitivity, short stature syndrome
  • Mandibular cleft
  • Hip pathological dislocation
  • aarskogs syndrome
  • Spherophakia
  • Degenerative amsterodamensis typus
  • Noonan-Ehmke syndrome
  • Genetic syndromic childhood obesity
  • Dwarfism, Silver-Russell
  • Seckel Syndrome
  • Dwarfism-ichthyosiform erythroderma-mental deficiency syndrome
  • Turner phenotype, karyotype normal
  • Heritable disorder of neutrophil function
  • Angioma pigmentosum atrophicum
  • Russell Silver Syndrome
  • Larsen-like osseous dysplasia, short stature syndrome
  • Intellectual disability and short stature with hand contracture and genital anomaly syndrome
  • Deafness with epiphyseal dysplasia and short stature syndrome
  • Short stature with craniofacial anomalies and genital hypoplasia syndrome
  • Oliver McFarlane syndrome
  • Congenital bowing of tibia and/or fibula
  • BIDS syndrome
  • ACD (alopecia, contracture, dwarfism) mental retardation syndrome
  • Blakemore Durmaz Vasileiou syndrome
  • Pierre Robin syndrome
  • Cockayne syndrome type 3
  • FAO - Fatty alcohol-nicotinamide adenine dinucleotide oxidase-reductase deficiency
  • Dwarfism-eczema-peculiar facies syndrome
  • Multiple malformation syndrome, moderate short stature, facial
  • Microphakia
  • Lysine methyltransferase 2D-related choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome
  • Brachydactyly, short stature, retinitis pigmentosa syndrome
  • Short stature Brussels type
  • Congenital abnormal shape of frontal bone
  • Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome
  • Richieri Costa Pereira syndrome
  • Seckel-Type Dwarfism
  • 6q16 microdeletion syndrome
  • Mievis Verellen Dumoulin syndrome
  • Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
  • Multiple malformation syndrome with senile-like appearance
  • Trigonocephaly
  • Chronic deafness
  • Prader-Willi-like syndrome due to microdeletion 6q16
  • Microphthalmia with colobomatous cyst
  • noonans syndrome
  • Noonan syndrome-like disorder with loose anagen hair
  • mulvihill smith syndrome
  • Absent thumb with short stature and immunodeficiency syndrome
  • Congenital malformation syndromes associated with short stature
  • SHOX-related short stature
  • seckel's syndrome
  • lange syndrome cornelia de
  • cornelia de langes syndrome
  • Congenital abnormal shape of tibia
  • Robin sequence
  • Trichomegaly with retina pigmentary degeneration and dwarfism syndrome
  • Congenital atresia of choana
  • Congenital spherophakia
  • MAGEL2-related Prader-Willi-like syndrome
  • Prader-Willi-like syndrome
  • Xeroderma of Kaposi
  • Russell-Silver syndrome (disorder)
  • Atresia of posterior nares
  • Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome
  • Trigonocephalus
  • Amish brittle hair syndrome
  • Nanocephalic dwarf
  • Congenital misshapen tibia
  • Pseudo Ullrich Turner Syndrome
  • Hereditary opalescent dentin
  • Carboxypeptidase E-related Prader-Willi-like syndrome
  • Cutaneous mastocytosis, short stature, hearing loss syndrome
  • BDV syndrome
  • Volcke Soekarman syndrome
  • AARSKOG SYNDROME, X-LINKED
  • Goniodysgenesis with mental deficiency and short stature
  • Atrophoderma pigmentosum
  • Autosomal recessive Robinow syndrome
  • Congenital small lens
  • Classical Cockayne syndrome
  • russell syndrome
  • Noonan Ehmke Syndrome
  • Schaaf Yang syndrome
  • SRS
  • Pierre Robin association
  • Syndrome, Progeria-Like
  • greig syndrome
  • Robinow Silverman Smith syndrome
  • X-linked colobomatous microphthalmia, microcephaly, short stature, psychomotor retardation syndrome
  • Bruck-de Lange syndrome
  • silvers syndrome
  • familial syndrome turners
  • Dysmorphism, short stature, deafness, pseudohermaphroditism syndrome
  • Bent bone dysplasia group
  • Defect of vertebral segmentation
  • BDLS
  • Microphthalmos co-occurrent with congenital ocular coloboma
  • Deletion of part of chromosome 6
  • Tosti syndrome
  • De Lange syndrome (disorder)
  • syndrome cornelia de lange
  • Micrognathia-glossoptosis syndrome
  • Syndrome, Russell Silver
  • Short stature with webbed neck and congenital heart disease syndrome
  • Alopecia, contracture, dwarfism, intellectual disability syndrome
Frequently Asked Questions
What is the ICD-10 code for other congen malform synd predom assoc with short stature?

The ICD-10-CM code for other congen malform synd predom assoc with short stature is Q87.19. The full clinical description is "Other congenital malformation syndromes predominantly associated with short stature". Q87.19 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q87.19 mean?

ICD-10-CM code Q87.19 represents “Other congenital malformation syndromes predominantly associated with short stature”. 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 Q87.19 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, also report: code(s) to identify all associated manifestations.

What SNOMED CT codes does Q87.19 map to?

Q87.19 maps to 118 SNOMED CT concepts: 783551005, 1003380001, 720979002, 14921002, 719685004, 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.

How does Q87.19 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congen malform synd predom assoc with short stature 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 Q87.19?

There is no direct ICD-11 mapping available for Q87.19 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.