Q74.8
BillableOther specified congenital malformations of limb(s)
Other specified congenital malformations of limb(s)
Status
Billable / Specific
Parent Code
Q74Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Anisomelia2107001
- Congenital anomaly of macula4041005
- Micrognathia-glossoptosis syndrome4602007
- Pierre Robin association4602007
- Pierre Robin syndrome4602007
- Robin sequence4602007
- Congenital webbing of neck11731003
- Neck webbing11731003
- Webbed neck11731003
- CDH - Congenital diaphragmatic hernia17190001
- Congenital diaphragmatic hernia17190001
- Congenital absence of proximal portion of limb22841008
- Phocomelia22841008
- Phocomelic dwarf22841008
- Congenital dilatation of colon24291004
- Congenital megacolon24291004
- Notomelus29328001
- Akinesia33994004
- Congenital duplication of limb34488005
- Dimelia34488005
- Chicken breast38774000
- Keeled chest38774000
- Pectus carinatum38774000
- Pigeon breast38774000
- Pigeon chest38774000
- Brachyphalangia38998004
- Symbrachydactyly41878001
- Congenital hypotrichia56558005
- Congenital hypotrichosis56558005
- Hypotrichosis congenita56558005
- Arachnodactyly62250003
- Congenital arachnodactyly62250003
- Spider finger62250003
- Larsen syndrome63387002
- Brachydactyly syndrome type E63711009
- Congenital humpback71311003
- Congenital hunchback71311003
- Congenital kyphosis71311003
- Congenital absence of tibia79177001
- Tibial hemimelia79177001
- Polymelia89243009
- Congenital abnormal shape of digit92907008
- Congenital abnormal shape of rib92943002
- Congenital misshapen rib92943002
- Mis-shapen ribs92943002
- Congenital hyperextension of limb93095003
- Macromelia93180003
- Macromelus93180003
- Congenital hyperflexion of limb93232005
- Congenital malposition of digit93317000
- Congenital malrotation of limb93367007
- Microdactylia94685002
- Microdactyly94685002
- Dentinogenesis imperfecta196286005
- Hereditary opalescent dentin196286005
- Congenital pectus carinatum205101001
- Duplication of whole limb205284003
- Brachymesophalangia205317004
- Multiple pterygium syndrome205819008
- Megakaryocytic thrombocytopenia234483004
- Hereditary camptodactyly238855000
- Bifid digit253971008
- Partial duplication of digit253971008
- Congenital deformity of lumbosacral region254033007
- Kyphosis deformity of thoracic spine298493002
- Kyphosis of dorsal spine298493002
- Kyphosis of thoracic spine298493002
- Deformity of sternum298727009
- Congenital kyphoscoliosis405772002
- Pseudarthrosis410818009
- Pseudoarthrosis410818009
- Myxoma of heart426191007
- Pectus deformity of chest444693004
- Congenital hernia of foramen of Bochdalek447821002
- Congenital posterolateral diaphragmatic hernia447821002
- Pleuroperitoneal hernia447821002
- Hereditary dysplasia of blood vessel461415008
- Anophthalmia-Waardenburg syndrome703403003
- Anophthalmia-syndactyly703403003
- Anophthalmos with limb anomalies703403003
- Anophthalmos-limb anomalies syndrome703403003
- Microphthalmia with limb anomalies703403003
- Ophthalmo-acromelic syndrome703403003
- Ophthalmoacromelic syndrome703403003
- Syndactyly-anophthalmos syndrome703403003
- Waardenburg anophthalmia syndrome703403003
- Aplasia of fibula co-occurrent with complex brachydactyly715474004
- Fibular aplasia and complex brachydactyly715474004
- Du Pan syndrome715474004
- OMM (ophthalmomandibulomelic) syndrome715484003
- Ophthalmomandibulomelic dysplasia715484003
- Pillay syndrome715484003
- Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome715506001
- Stoll Lévy Francfort syndrome715506001
- Aplasia of tibia with split hand split foot deformity715531000
- Split hand foot malformation with long bone deficiency715531000
- Tibial aplasia and ectrodactyly syndrome715531000
- Tibial hemimelia ectrodactyly syndrome715531000
- Brachydactyly Farabee type715720006
- Brachydactyly type A1715720006
- Brachydactyly Temtamy type715721005
- Brachydactyly type A4715721005
- Brachydactyly type A6715722003
- Osebold Remondini syndrome715722003
- Aminopterin syndrome-like sine aminopterin715867000
- Pseudoaminopterin syndrome715867000
- Acrocallosal syndrome715951007
- Camptodactyly with joint contracture and facial skeletal defect syndrome715986009
- Rozin Hertz Goodman syndrome715986009
- Rozin camptodactyly syndrome715986009
- Congenital bowing of long bone716098006
- Seaver Cassidy syndrome716337006
- MONA (multicentric osteolysis nodulosis arthropathy) spectrum716868003
- Multicentric osteolysis nodulosis arthropathy spectrum716868003
- Familial digital arthropathy and brachydactyly syndrome717192003
- 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
- Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome717823001
- Goldblatt chondrodysplasia717823001
- Goldblatt syndrome717823001
- Odontochondrodysplasia717823001
- Grange occlusive arterial syndrome717824007
- Grange syndrome717824007
- Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome717824007
- Khalifa Graham syndrome719256004
- Pterygium colli with intellectual disability and digital anomaly syndrome719256004
- Castro Gago Pombo Novo syndrome719377004
- Microcephalus with albinism and digital anomaly syndrome719377004
- Microcephaly with albinism and digital anomaly syndrome719377004
- Microcephalus with brachydactyly and kyphoscoliosis syndrome719378009
- Microcephaly with brachydactyly and kyphoscoliosis syndrome719378009
- Viljoen Kallis Voges syndrome719378009
- Lethal Larsen-like syndrome719409004
- Stoll Kieny Dott syndrome719823007
- Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome719823007
- Morava Mehes syndrome719843001
- Ulna fibula ray defect and brachydactyly syndrome719843001
- Acro-fronto-facio-nasal dysostosis720408003
- Acrofrontofacionasal dysostosis720408003
- Richieri Costa Colletto syndrome720408003
- Acrocephalopolydactylous dysplasia720417003
- Acrocephalopolydactyly720417003
- Elejalde syndrome720417003
- Acrocraniofacial dysostosis720418008
- Kaplan Plauchu Fitch syndrome720418008
- Acrofacial dysostosis Kennedy Teebi type720427009
- Kennedy Teebi syndrome720427009
- Acrofacial dysostosis Palagonia type720429007
- Arachnodactyly with abnormal ossification and intellectual disability syndrome720501007
- Kosztolanyi syndrome720501007
- Arachnodactyly and intellectual disability with facial dysmorphism syndrome720502000
- De Die, Smulders, Vles, Fryns syndrome720502000
- Bilginturan brachydactyly720568003
- Bilginturan syndrome720568003
- Brachydactyly and arterial hypertension syndrome720568003
- Brachydactyly type E with short stature and hypertension720568003
- Brachydactyly Smorgasbord type720571006
- Brachydactyly type A7720571006
- BOD (brachymorphism, onychodysplasia, dysphalangism) syndrome720573009
- Brachymorphism with onychodysplasia and dysphalangism syndrome720573009
- Senior syndrome720573009
- EEM (ectodermal dysplasia, ectrodactyly, macular dystrophy) syndrome720856002
- EEM syndrome720856002
- Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome720856002
- Diaphragmatic defect, limb deficiency, skull defect syndrome721095007
- Froster Huch syndrome721095007
- Hirschsprung disease with type D brachydactyly syndrome721222007
- Daish Hardman Lamont syndrome732926009
- Hydrocephalus, tall stature, joint laxity syndrome732926009
- Hydrocephaly, tall stature, joint laxity syndrome732926009
- Dysmorphism, pectus carinatum, joint laxity syndrome733038005
- Guízar Vázquez Sánchez Manzano syndrome733038005
- Camptobrachydactyly733045005
- Congenital conductive hearing loss737344003
- X-linked lethal multiple pterygium syndrome763462004
- Intellectual disability, spasticity, ectrodactyly syndrome763743003
- Jancar syndrome763743003
- Intellectual disability, brachydactyly, Pierre Robin syndrome763744009
- Keipert syndrome763774001
- Nasodigitoacoustic syndrome763774001
- Cryptorchidism, arachnodactyly, intellectual disability syndrome764950001
- Van Benthem Driessen Hanveld syndrome764950001
- Dyssegmental dysplasia Silverman Handmaker type765204000
- Brachydactyly, mesomelia, intellectual disability, heart defect syndrome765761009
- Stratton Garcia Young syndrome765761009
- Carney complex variant766881008
- Carney complex, trismus, pseudocamptodactyly syndrome766881008
- Autosomal dominant multiple pterygium syndrome771269000
- Distal arthrogryposis type 8771269000
- SOFT (short stature, onychodysplasia, facial dysmorphism, hypotrichosis) syndrome773625007
- SOFT syndrome773625007
- Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome773625007
- Congenital pseudoarthrosis of limb782689003
- Brachydactyly type D890439005
- Broad shaped phalanx896775003
- Congenital abnormal broad shape of phalanx896775003
- Abnormally short distal phalanx of thumb897340006
- Shortened distal phalanx of thumb897340006
- Abnormally short phalanx of thumb897342003
- Shortened phalanx of thumb897342003
- Abnormally short distal phalanx of great toe897452003
- Short distal phalanx of first toe897452003
- Short distal phalanx of hallux897452003
- Abnormally short distal phalanx of foot897457009
- Short distal phalanx of toe897457009
- Abnormally short great toe897460002
- Short first toe897460002
- Short hallux897460002
- Abnormally short phalanx of great toe897466008
- Short phalanx of first toe897466008
- Short phalanx of hallux897466008
- Congenital corneal dystrophy1003408005
- Congenital dystrophy of cornea1003408005
- Mesomelic dysplasia of upper limb1010609002
- Congenital dysplasia of radius1142185008
- Congenital dysplasia of nail unit1142193008
- Aplasia of fibula1145459008
- Aplasia of tibia1145471002
- Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome1172685001
- Macrothrombocytopenia, lymphoedema, developmental delay, facial dysmorphism, camptodactyly syndrome1172685001
- Takenouchi Kosaki syndrome1172685001
- Congenital muscular dystrophy Davignon Chauveau type1172688004
- Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome1172688004
- Al Gazali Al Talabani syndrome1208342001
- Al Gazali Lytle syndrome1208342001
- Eye defects, arachnodactyly, cardiopathy syndrome1208342001
- Severe myopia, generalised joint laxity, short stature syndrome1217372003
- Severe myopia, generalized joint laxity, short stature syndrome1217372003
- CLIFAHDD (congenital limbs, face contractures, hypotonia, developmental delay) syndrome1255322002
- CLIFAHDD syndrome1255322002
- Congenital contracture of limbs and face, hypotonia, developmental delay syndrome1255322002
- Body height below reference range1363478003
- Congenital kyphosis of thoracic spine305141000119101
Frequently Asked Questions
What is the ICD-10 code for other specified congenital malformations of limb(s)?
The ICD-10-CM code for other specified congenital malformations of limb(s) is Q74.8. The full clinical description is "Other specified congenital malformations of limb(s)". Q74.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q74.8 mean?
ICD-10-CM code Q74.8 represents "Other specified congenital malformations of limb(s)". 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 Q74.8 a billable code?
Yes, Q74.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q74.8 in?
Q74.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q74.8?
Q74.8 has Excludes1 notes indicating codes that cannot be used together with it, including: polydactyly (Q69.-); reduction defect of limb (Q71-Q73); syndactyly (Q70.-).
What SNOMED CT codes does Q74.8 map to?
Q74.8 maps to 118 SNOMED CT concepts: 897457009, 897452003, 897340006, 897460002, 897466008, and 113 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q74.8?
Q74.8 is linked to 1 UMLS Concept Unique Identifier: C0478072. 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.