Diagnosis Code: Q15.9

Short Description: Congenital malformation of eye, unspecified

Long Description: Congenital malformation of eye, unspecified

The code Q15.9 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 eye (Q15)
      • Q15.9 Congenital malformation of eye, unspecified

Code Version: 2022 ICD-10-CM

Synonyms

• Acrorenoocular syndrome
• Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
• Aplasia cutis congenita secondary to malformation syndrome
• Auricular abnormality, cleft lip, ocular abnormality syndrome
• Axonal neuropathy
• Bilateral hearing loss
• Choanal atresia
• Chronic diarrhea of infants AND/OR young children
• CODAS syndrome
• Combined malformation of central nervous system and skeletal muscle
• Conductive hearing loss of left ear
• Conductive hearing loss of right ear
• Conductive hearing loss, bilateral
• Congenital anomaly of eye
• Congenital anomaly of ocular adnexa
• Congenital atresia of nares
• Congenital atresia of nasopharynx
• Congenital atresia of pharynx
• Congenital hypotrichia
• Congenital malformation of eye, ear and neck
• Congenital mixed conductive and sensorineural hearing loss
• Dysplasia with defective mineralization
• Familial aplasia of the vermis
• Feingold syndrome
• Frontonasal dysplasia sequence
• Glaucoma due to congenital anomaly of eye
• Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome
• Hereditary cerebellar atrophy
• Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome
• Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome
• Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome
• Intractable diarrhea with choanal atresia and eye anomaly syndrome
• Joubert syndrome
• Joubert syndrome with oculorenal defect
• Left conductive hearing loss
• Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
• Manitoba oculotrichoanal syndrome
• Matthew Wood syndrome
• Mixed conductive AND sensorineural hearing loss
• Mixed conductive and sensorineural hearing loss of left ear
• Mixed conductive and sensorineural hearing loss of right ear
• Mixed conductive and sensorineural hearing loss, bilateral
• MOMO syndrome
• Muscle eye brain disease with bilateral multicystic leukodystrophy
• Nephronophthisis
• Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome
• Ocular anomalies, axonal neuropathy, developmental delay syndrome
• Oculoauricular syndrome Schorderet type
• Oculoauriculofrontonasal syndrome
• Oculocerebrocutaneous syndrome
• Oculocerebrodental syndrome
• Oculootoradial syndrome
• Oculopalatocerebral syndrome
• Ophthalmo-acromelic syndrome
• Persistent hyperplastic primary vitreous
• Pierson syndrome
• Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome
• Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
• RAB18 deficiency
• Sensorineural hearing loss of bilateral ears
• Steroid-resistant nephrotic syndrome
• Upper limb defect with eye and ear abnormalities syndrome

Diagnostic Related Group(s)

The code Q15.9 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 Q15.9 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital anomaly of eye
  • Congenital deformity of eye

Crosswalk Information

Similar Codes

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

« Previous Code