Diagnosis Code

Q35.9 CLEFT PALATE, UNSPECIFIED


Code Information

Diagnosis Code: Q35.9

Short Description: Cleft palate, unspecified

Long Description: Cleft palate, unspecified

The code Q35.9 is VALID for claim submission

Code Classification:

  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Cleft lip and cleft palate (Q35-Q37)
      • Cleft palate (Q35)
        • Q35.9 Cleft palate, unspecified

Code Version: 2022 ICD-10-CM


Synonyms

  • Abruzzo Erickson syndrome
  • Acrocardiofacial syndrome
  • Ankyloblepharon
  • Ankyloblepharon filiforme adnatum
  • Ankyloblepharon filiforme adnatum with cleft palate syndrome
  • Bilateral cleft of primary palate
  • Bilateral congenital malformation of ears
  • Bilateral congenital malformation of external ears
  • Bilateral microtia with deafness and cleft palate syndrome
  • Cholestasis with pigmentary retinopathy and cleft palate syndrome
  • Cleft of primary palate
  • Cleft palate
  • Cleft palate lateral synechia syndrome
  • Cleft palate with short stature and vertebral anomaly syndrome
  • Cleft palate with stapes fixation and oligodontia syndrome
  • Cleft palate, large ears, small head syndrome
  • Congenital ankyloblepharon
  • Congenital anomaly of macula
  • Congenital anomaly of ossicles of ear
  • Congenital cleft hand
  • Congenital coloboma of macula lutea
  • Congenital fusion of ossicles of ear
  • Congenital hallux valgus
  • Congenital mixed conductive and sensorineural hearing loss
  • Congenital omphalocele
  • Congenital retrognathism
  • Congenital umbilical hernia
  • Facial dysmorphism, cleft palate, loose skin syndrome
  • Genitopalatocardiac syndrome
  • Holzgreve syndrome
  • Incomplete bilateral cleft palate
  • Incomplete cleft palate
  • Lethal omphalocele with cleft palate syndrome
  • Macrosomia, microphthalmia, cleft palate syndrome
  • Macrotia
  • Macular coloboma, cleft palate, hallux valgus syndrome
  • Microcephalus cleft palate syndrome
  • Microtia
  • Mixed conductive AND sensorineural hearing loss
  • Oligodontia
  • Poikiloderma, alopecia, retrognathism, cleft palate syndrome
  • Potter's facies
  • Pure gonadal dysgenesis
  • Pure gonadal dysgenesis 46,XY
  • Reardon Hall Slaney syndrome
  • Renal agenesis
  • Retinal pigment deposits
  • Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome
  • Submucous cleft palate
  • Tongue tie
  • Velopharyngeal inadequacy
  • Velopharyngeal incompetence
  • Velopharyngeal incompetence due to cleft palate
  • X-linked cleft palate and ankyloglossia
  • X-linked sensorineural hearing loss

References to Index of Diseases and Injuries

The code Q35.9 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Cleft palate NOS

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
Q35.9 Right Arrow 749.00 Cleft palate NOS

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
Q35 Cleft palate
Q35.1 Cleft hard palate
Q35.3 Cleft soft palate
Q35.5 Cleft hard palate with cleft soft palate
Q35.7 Cleft uvula


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