Diagnosis Code: Q11.2

Short Description: Microphthalmos

Long Description: Microphthalmos

The code Q11.2 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)
    • Anophthalmos, microphthalmos and macrophthalmos (Q11)
      • Q11.2 Microphthalmos

Code Version: 2022 ICD-10-CM

Synonyms

• Akinesia
• Ankyloblepharon
• Arrhinia with choanal atresia and microphthalmia syndrome
• Bilateral cryptophthalmos
• Bilateral microphthalmos
• Bilateral microphthalmos
• Bilateral microphthalmos
• Bilateral microphthalmos with congenital coloboma
• Bilateral partial cryptophthalmos
• Central obesity
• Choanal atresia
• Colobomatous microphthalmia
• Colobomatous microphthalmia
• Colobomatous microphthalmia
• Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome
• Colobomatous microphthalmia, rhizomelic dysplasia syndrome
• Complete cryptophthalmos
• Congenital ankyloblepharon
• Congenital atresia of nares
• Congenital atresia of nasopharynx
• Congenital atresia of pharynx
• Congenital hypoplasia of nose
• Congenital prognathism
• Cryptophthalmos
• Drusen of optic disc
• Dysplasia of eye
• Frontonasal dysplasia sequence
• Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome
• Hypoplasia of eye
• Hypoplasia of eye
• Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome
• Isolated cryptophthalmos
• Lenz microphthalmia syndrome
• Macrosomia, microphthalmia, cleft palate syndrome
• Microphthalmia with ankyloblepharon and intellectual disability syndrome
• Microphthalmia with brain and digit anomaly
• Microphthalmia with brain atrophy syndrome
• Microphthalmia with linear skin defect syndrome
• Microphthalmia, microtia, fetal akinesia syndrome
• Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome
• Microphthalmic socket
• Microphthalmos
• Microphthalmos associated with other anomalies of eye AND/OR adnexa
• Microphthalmos due to branchio-oculo-facial syndrome
• Microphthalmos due to Delleman syndrome
• Microphthalmos due to Fryns syndrome
• Microphthalmos of left eye
• Microphthalmos of left eye
• Microphthalmos of left eye
• Microphthalmos of right eye
• Microphthalmos of right eye
• Microphthalmos of right eye
• Microtia
• MMEP syndrome
• Nanophthalmia
• Nanophthalmia
• Retinal degeneration, nanophthalmos, glaucoma syndrome
• Simple microphthalmos
• Syndromic microphthalmia type 5
• Syndromic nanophthalmos due to Kenny-Caffey syndrome
• X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome

Diagnostic Related Group(s)

The code Q11.2 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Other Disorders Of The Eye With Mcc Or Thrombolytic Agent (124)
• Other Disorders Of The Eye Without Mcc (125)

References to Index of Diseases and Injuries

The code Q11.2 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Cryptophthalmos NOS
  • Dysplasia of eye
  • Hypoplasia of eye
  • Rudimentary eye
• Type 1 Excludes Notes:
  • cryptophthalmos syndrome (@Q87.0*)

Crosswalk Information

Similar Codes

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

« Previous Code