Diagnosis Code: Q74.8

Short Description: Other specified congenital malformations of limb(s)

Long Description: Other specified congenital malformations of limb(s)

The code Q74.8 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
    • Other congenital malformations of limb(s) (Q74)
      • Q74.8 Other specified congenital malformations of limb(s)

Code Version: 2022 ICD-10-CM

Synonyms

• Absence of tibia
• Acrocallosal syndrome
• Acrocephalopolydactyly
• Acrocraniofacial dysostosis
• Acrofacial dysostosis Kennedy Teebi type
• Acrofacial dysostosis Palagonia type
• Acrofrontofacionasal dysostosis
• Akinesia
• Akinesia
• Anisomelia
• Arachnodactyly
• Arachnodactyly
• 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
• Brachymesophalangia
• Brachymorphism with onychodysplasia and dysphalangism syndrome
• Brachyphalangia
• Camptobrachydactyly
• Carney complex, trismus, pseudocamptodactyly syndrome
• CLAPO syndrome
• 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 hyperextension of limb
• Congenital hyperflexion of limb
• Congenital hypotrichia
• Congenital kyphoscoliosis
• Congenital kyphosis
• 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
• Cryptorchidism, arachnodactyly, intellectual disability syndrome
• Deformity of phalanx of toe
• Deformity of sternum
• 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
• 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
• 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

Diagnostic Related Group(s)

The code Q74.8 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
• Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
• Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

Crosswalk Information

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This page was last updated on: 10/1/2023

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