Anophthalmia-Waardenburg syndrome
Deformity of sternum
Congenital conductive hearing loss
Goldblatt chondrodysplasia
Shortened distal phalanx of thumb
Intellectual disability, spasticity, ectrodactyly syndrome
Aminopterin syndrome-like sine aminopterin
Tibial hemimelia
CLAPO syndrome
Brachydactyly Smorgasbord type
Short hallux
Short first toe
Duplication of whole limb
Kyphosis of thoracic spine
Pleuroperitoneal hernia
Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome
BOD (brachymorphism, onychodysplasia, dysphalangism) syndrome
Acrofacial dysostosis Kennedy Teebi type
Hirschsprung disease with type D brachydactyly syndrome
Congenital dilatation of colon
Arachnodactyly
Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome
Syndactyly-anophthalmos syndrome
Brachymesophalangia
Acrofrontofacionasal dysostosis
CLAPO (capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth) syndrome
Multiple pterygium syndrome
Brachydactyly type A7
Broad shaped phalanx
SOFT (short stature, onychodysplasia, facial dysmorphism, hypotrichosis) syndrome
Congenital bowing of long bone
Seaver Cassidy syndrome
Congenital abnormal shape of digit
Eye defects, arachnodactyly, cardiopathy syndrome
Grange occlusive arterial syndrome
Abnormally short great toe
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome
Congenital misshapen rib
Pectus deformity of chest
Daish Hardman Lamont syndrome
Shortened phalanx of thumb
Brachydactyly type E with short stature and hypertension
Dyssegmental dysplasia Silverman Handmaker type
Akinesia
Congenital absence of tibia
Polymelia
Waardenburg anophthalmia syndrome
CLIFAHDD (congenital limbs, face contractures, hypotonia, developmental delay) syndrome
Congenital abnormal shape of rib
Congenital anomaly of macula
Aplasia of fibula
Rozin camptodactyly syndrome
Congenital dysplasia of nail unit
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome
Familial digital arthropathy and brachydactyly syndrome
Congenital humpback
Spider finger
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome
Severe myopia, generalized joint laxity, short stature syndrome
Arachnodactyly and intellectual disability with facial dysmorphism syndrome
Congenital hypotrichosis
Congenital webbing of neck
Hydrocephaly, tall stature, joint laxity syndrome
Neck webbing
Congenital megacolon
Congenital pectus carinatum
Congenital kyphoscoliosis
Morava Mehes syndrome
Notomelus
Brachymorphism with onychodysplasia and dysphalangism syndrome
Camptodactyly with joint contracture and facial skeletal defect syndrome
Acrocraniofacial dysostosis
Hypotrichosis congenita
Brachydactyly type D
Larsen syndrome
Froster Huch syndrome
Tibial aplasia and ectrodactyly syndrome
Keipert syndrome
Abnormally short distal phalanx of foot
EEM syndrome
Megakaryocytic thrombocytopenia
OMM (ophthalmomandibulomelic) syndrome
Tibial hemimelia ectrodactyly syndrome
Khalifa Graham syndrome
Mis-shapen ribs
Congenital dysplasia of radius
Robin sequence
Congenital malrotation of limb
Pseudarthrosis
Hereditary dysplasia of blood vessel
Acrocephalopolydactylous dysplasia
Congenital arachnodactyly
Autosomal dominant multiple pterygium syndrome
Carney complex, trismus, pseudocamptodactyly syndrome
Al Gazali Al Talabani syndrome
Mesomelic dysplasia of upper limb
Congenital hernia of foramen of Bochdalek
Congenital posterolateral diaphragmatic hernia
Macrothrombocytopenia, lymphoedema, developmental delay, facial dysmorphism, camptodactyly syndrome
Microdactyly
Pectus carinatum
Severe myopia, generalised joint laxity, short stature syndrome
Jancar syndrome
Partial duplication of digit
Rozin Hertz Goodman syndrome
Ulna fibula ray defect and brachydactyly syndrome
Van Benthem Driessen Hanveld syndrome
Keeled chest
Camptobrachydactyly
Stratton Garcia Young syndrome
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome
Short phalanx of first toe
Brachydactyly, mesomelia, intellectual disability, heart defect syndrome
Congenital corneal dystrophy
Diaphragmatic defect, limb deficiency, skull defect syndrome
Anophthalmos with limb anomalies
Abnormally short phalanx of great toe
Osebold Remondini syndrome
De Die, Smulders, Vles, Fryns syndrome
Abnormally short distal phalanx of great toe
Dentinogenesis imperfecta
Microcephalus with albinism and digital anomaly syndrome
Microcephalus with brachydactyly and kyphoscoliosis syndrome
Acrocephalopolydactyly
Arachnodactyly with abnormal ossification and intellectual disability syndrome
Dysmorphism, pectus carinatum, joint laxity syndrome
Congenital hypotrichia
Bilginturan brachydactyly
Congenital abnormal broad shape of phalanx
Hereditary camptodactyly
Aplasia of fibula co-occurrent with complex brachydactyly
Congenital muscular dystrophy Davignon Chauveau type
MONA (multicentric osteolysis nodulosis arthropathy) spectrum
Hereditary opalescent dentin
Macromelus
Short distal phalanx of toe
Short phalanx of hallux
Body height below reference range
Brachyphalangia
Castro Gago Pombo Novo syndrome
Senior syndrome
Congenital hyperflexion of limb
Ophthalmomandibulomelic dysplasia
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome
Pillay syndrome
Multicentric osteolysis nodulosis arthropathy spectrum
Myxoma of heart
Lethal Larsen-like syndrome
Grange syndrome
Goldblatt syndrome
Acrocallosal syndrome
Anophthalmia-syndactyly
Congenital hyperextension of limb
Acro-fronto-facio-nasal dysostosis
Elejalde syndrome
Congenital hunchback
Microdactylia
Congenital kyphosis
Richieri Costa Colletto syndrome
Pseudoaminopterin syndrome
Kyphosis of dorsal spine
Stoll Lévy Francfort syndrome
Brachydactyly syndrome type E
Brachydactyly Farabee type
Dimelia
Distal arthrogryposis type 8
Takenouchi Kosaki syndrome
Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome
EEM (ectodermal dysplasia, ectrodactyly, macular dystrophy) syndrome
Odontochondrodysplasia
Brachydactyly type A6
Guízar Vázquez Sánchez Manzano syndrome
Intellectual disability, brachydactyly, Pierre Robin syndrome
Brachydactyly type A1
Pierre Robin association
Abnormally short phalanx of thumb
Congenital duplication of limb
Short distal phalanx of first toe
Anophthalmos-limb anomalies syndrome
Chicken breast
Kaplan Plauchu Fitch syndrome
Stoll Kieny Dott syndrome
Viljoen Kallis Voges syndrome
Fibular aplasia and complex brachydactyly
Phocomelia
Congenital malposition of digit
Capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth syndrome
Microcephaly with brachydactyly and kyphoscoliosis syndrome
Congenital pseudoarthrosis of limb
Hydrocephalus, tall stature, joint laxity syndrome
Cryptorchidism, arachnodactyly, intellectual disability syndrome
Nasodigitoacoustic syndrome
Aplasia of tibia with split hand split foot deformity
Du Pan syndrome
Bifid digit
Microcephaly with albinism and digital anomaly syndrome
Symbrachydactyly
Webbed neck
Pseudoarthrosis
Pterygium colli with intellectual disability and digital anomaly syndrome
Kyphosis deformity of thoracic spine
Kennedy Teebi syndrome
Pigeon chest
Congenital deformity of lumbosacral region
Microphthalmia with limb anomalies
Macromelia
Carney complex variant
SOFT syndrome
Brachydactyly type A4
Kosztolanyi syndrome
CLIFAHDD syndrome
Congenital kyphosis of thoracic spine
Anisomelia
Aplasia of tibia
Phocomelic dwarf
Pigeon breast
CDH - Congenital diaphragmatic hernia
Acrofacial dysostosis Palagonia type
Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome
Pierre Robin syndrome
Ophthalmo-acromelic syndrome
Al Gazali Lytle syndrome
Brachydactyly Temtamy type
Congenital diaphragmatic hernia
Congenital dystrophy of cornea
Micrognathia-glossoptosis syndrome
Congenital absence of proximal portion of limb
Ophthalmoacromelic syndrome
Short distal phalanx of hallux
Split hand foot malformation with long bone deficiency
X-linked lethal multiple pterygium syndrome
Abnormally short distal phalanx of thumb
Bilginturan syndrome
Brachydactyly and arterial hypertension syndrome

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.

How does Q74.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified congenital malformations of limb(s) 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 Q74.8?

Q74.8 maps to the ICD-11 code: LB9Z (Structural developmental anomalies of the skeleton, unspecified).

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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.