Diagnosis Code: Q69.9

Short Description: Polydactyly, unspecified

Long Description: Polydactyly, unspecified

The code Q69.9 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)
    • Polydactyly (Q69)
      • Q69.9 Polydactyly, unspecified

Code Version: 2022 ICD-10-CM

Synonyms

• Absent tibia, polydactyly, arachnoid cyst syndrome
• Arachnoid cyst
• Autosomal dominant polycystic kidney disease
• Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome
• Brain malformation, congenital heart disease, postaxial polydactyly syndrome
• Congenital abnormal shape of rib
• Congenital anomaly of lobe of ear
• Congenital dilatation of colon
• Congenital hypoplasia of tibia
• Congenital lymphangiectasia
• Congenital malformation of the meninges
• Congenital pectus excavatum
• Cortical blindness
• Cortical blindness, intellectual disability, polydactyly syndrome
• Dandy-Walker malformation with postaxial polydactyly syndrome
• Dandy-Walker syndrome
• Deformity of sternum
• Ectrodactyly polydactyly syndrome
• Finger hyperphalangy, toe anomalies, severe pectus excavatum syndrome
• Hereditary disorder of lymphatic system
• Hexadactyly
• Hirschsprung disease with deafness and polydactyly syndrome
• Holoprosencephaly and postaxial polydactyly syndrome
• Holzgreve syndrome
• Hyperphalangy
• Hyperphalangy
• Hypoplastic tibia and postaxial polydactyly syndrome
• Intellectual disability, polydactyly, uncombable hair syndrome
• Macroencephaly
• McKusick Kaufman syndrome
• Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome
• Micromelia
• Mirror polydactyly, vertebral segmentation and limb defect syndrome
• Mirror-image polydactyly
• Mullerian remnant
• Multinodular goiter
• Multinodular goiter, cystic kidney, polydactyly syndrome
• Oliver syndrome
• Pectus deformity of chest
• Pectus excavatum
• Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome
• Polydactyly
• Polydactyly myopia syndrome
• Postaxial polydactyly, anterior pituitary anomalies, facial dysmorphism syndrome
• Postaxial polydactyly, dental, vertebral anomalies syndrome
• Potter's facies
• Preaxial polydactyly, colobomata, intellectual disability syndrome
• Renal agenesis
• Scalp defect postaxial polydactyly syndrome
• Sensorineural hearing loss of bilateral ears
• Short rib dysplasia
• Short rib dysplasia
• Short rib dysplasia
• Short rib dysplasia
• Short rib dysplasia
• Short rib polydactyly syndrome
• Short rib polydactyly syndrome Saldino Noonan type
• Short rib-polydactyly syndrome, Majewski type
• Split foot
• Split-foot malformation, mesoaxial polydactyly syndrome
• Syndactyly, polydactyly, ear lobe syndrome
• Type III short rib polydactyly syndrome
• Type IV short rib polydactyly syndrome

Diagnostic Related Group(s)

The code Q69.9 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)

References to Index of Diseases and Injuries

The code Q69.9 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Supernumerary digit(s) NOS

Crosswalk Information

Similar Codes

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

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