Diagnosis Code: Q17.2

Short Description: Microtia

Long Description: Microtia

The code Q17.2 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Congenital malformations of eye, ear, face and neck (Q10-Q18)
    • Other congenital malformations of ear (Q17)
      • Q17.2 Microtia

Code Version: 2022 ICD-10-CM

Synonyms

• Akinesia
• Atresia of nasolacrimal duct
• Bilateral congenital malformation of ears
• Bilateral congenital malformation of external ears
• Bilateral microphthalmos
• Bilateral microtia with deafness and cleft palate syndrome
• Brachymesophalangia
• Complete deafness
• Congenital deafness
• Congenital deafness with labyrinthine aplasia, microtia and microdontia
• Cryptomicrotia brachydactyly syndrome
• Ear, patella, short stature syndrome
• Hypertelorism
• Hypertelorism with microtia and facial clefting syndrome
• Microdontia
• Microphthalmia, microtia, fetal akinesia syndrome
• Microphthalmos of left eye
• Microphthalmos of right eye
• Microtia
• Microtia
• Microtia
• Microtia
• Microtia
• Microtia
• Microtia, eye coloboma, imperforation of nasolacrimal duct syndrome

Diagnostic Related Group(s)

The code Q17.2 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Other Ear, Nose, Mouth And Throat Diagnoses With Mcc (154)
• Other Ear, Nose, Mouth And Throat Diagnoses With Cc (155)
• Other Ear, Nose, Mouth And Throat Diagnoses Without Cc/mcc (156)

Crosswalk Information

Similar Codes

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

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