2027 ICD-10-CM Diagnosis Code Q74.8Other specified congenital malformations of limb(s)

Alternate terms and clinical phrases that map to this code.

• Abnormally short distal phalanx of foot
• Abnormally short distal phalanx of great toe
• Abnormally short distal phalanx of thumb
• Abnormally short great toe
• Abnormally short phalanx of great toe
• Abnormally short phalanx of thumb
• Acrocallosal syndrome
• Acrocephalopolydactyly
• Acrocraniofacial dysostosis
• Acrofacial dysostosis Kennedy Teebi type
• Acrofacial dysostosis Palagonia type
• Acrofrontofacionasal dysostosis
• Akinesia
• Anisomelia
• Aplasia of fibula
• Aplasia of tibia
• Arachnodactyly
• Arachnodactyly and intellectual disability with facial dysmorphism syndrome
• Arachnodactyly with abnormal ossification and intellectual disability syndrome
• Autosomal dominant multiple pterygium syndrome
• Bifid digit
• Brachydactyly and arterial hypertension syndrome
• Brachydactyly syndrome type E
• Brachydactyly type A1
• Brachydactyly type A4
• Brachydactyly type A6
• Brachydactyly type A7
• Brachydactyly type D
• Brachydactyly, mesomelia, intellectual disability, heart defect syndrome
• Brachymesophalangia
• Brachymorphism with onychodysplasia and dysphalangism syndrome
• Brachyphalangia
• Camptobrachydactyly
• Carney complex, trismus, pseudocamptodactyly syndrome
• CLAPO syndrome
• Congenital abnormal broad shape of phalanx
• Congenital abnormal shape of digit
• Congenital abnormal shape of rib
• Congenital absence of tibia
• Congenital anomaly of macula
• Congenital bowing of long bone
• Congenital conductive hearing loss
• Congenital contracture of limbs and face, hypotonia, developmental delay syndrome
• Congenital corneal dystrophy
• Congenital deformity of lumbosacral region
• Congenital diaphragmatic hernia
• Congenital dilatation of colon
• Congenital dysplasia of nail unit
• Congenital dysplasia of radius
• Congenital hyperextension of limb
• Congenital hyperflexion of limb
• Congenital hypotrichia
• Congenital kyphoscoliosis
• Congenital kyphosis
• Congenital kyphosis of thoracic spine
• Congenital malposition of digit
• Congenital malrotation of limb
• Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome
• Congenital pectus carinatum
• Congenital posterolateral diaphragmatic hernia
• Congenital pseudoarthrosis of limb
• Congenital scoliosis deformity of spine
• Cryptorchidism, arachnodactyly, intellectual disability syndrome
• Dentinogenesis imperfecta
• Diaphragmatic defect, limb deficiency, skull defect syndrome
• Dimelia
• Duplication of whole limb
• Dysmorphism, pectus carinatum, joint laxity syndrome
• Dyssegmental dysplasia Silverman Handmaker type
• Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome
• Eye defects, arachnodactyly, cardiopathy syndrome
• Familial digital arthropathy and brachydactyly syndrome
• Fibular aplasia and complex brachydactyly
• Goldblatt syndrome
• Grange syndrome
• Hereditary camptodactyly
• Hereditary dysplasia of blood vessel
• Hirschsprung disease with type D brachydactyly syndrome
• Hydrocephalus, tall stature, joint laxity syndrome
• Intellectual disability, brachydactyly, Pierre Robin syndrome
• Intellectual disability, spasticity, ectrodactyly syndrome
• Keipert syndrome
• Kyphosis of thoracic spine
• Larsen syndrome
• Lethal Larsen-like syndrome
• Macromelia
• Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome
• Megakaryocytic thrombocytopenia
• Mesomelic dysplasia of upper limb
• Microcephalus with albinism and digital anomaly syndrome
• Microcephalus with brachydactyly and kyphoscoliosis syndrome
• Microdactyly
• Morava Mehes syndrome
• Multicentric osteolysis nodulosis arthropathy spectrum
• Multiple pterygium syndrome
• Myxoma of heart
• Neck webbing
• Notomelus
• Ophthalmo-acromelic syndrome
• Ophthalmomandibulomelic dysplasia
• Pectus carinatum
• Pectus deformity of chest
• Phocomelia
• Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome
• Polymelia
• Pseudoaminopterin syndrome
• Pseudoarthrosis
• Pterygium colli with intellectual disability and digital anomaly syndrome
• Robin sequence
• Rozin Hertz Goodman syndrome
• Seaver Cassidy syndrome
• Severe myopia, generalized joint laxity, short stature syndrome
• Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome
• Symbrachydactyly
• Tibial aplasia and ectrodactyly syndrome
• Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome
• X-linked lethal multiple pterygium syndrome

Instructions from the official ICD-10-CM Tabular List that apply to Q74.8: its own notes plus those printed at Q74 and Chapter 17. A note printed at a category, block or chapter applies to every code under it.

Source: CMS ICD-10-CM Tabular List. How to read instructional notes.

Instructional notes printed at other codes that name Q74.8, its category, or a range that includes it.

Alphabetical index entries that point to this code.

• Absence (of) (organ or part) (complete or partial)

  • joint

    • congenital NEC Q74.8

• Accessory (congenital)

  • sesamoid bones Q74.8

• Anomaly, anomalous (congenital) (unspecified type) Q89.9

  • joint Q74.9

    • specified NEC Q74.8

• Dysplasia See Also: Anomaly;

  • joint, congenital Q74.8

• Fusion, fused (congenital)

  • joint (acquired) See Also: Ankylosis;

    • congenital Q74.8

  • limb, congenital Q74.8

• Larsen's syndrome (flattened facies and multiple congenital dislocations) Q74.8

• Malformation (congenital) See Also: Anomaly;

  • joint Q74.9

    • specified type NEC Q74.8

• Relaxation

  • joint (capsule) (ligament) (paralytic) See: Flail, joint;

    • congenital NEC Q74.8

• Syndrome See Also: Disease;

  • Larsen's Q74.8