Diagnosis Code: Q18.9

Short Description: Congenital malformation of face and neck, unspecified

Long Description: Congenital malformation of face and neck, unspecified

The code Q18.9 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 face and neck (Q18)
      • Q18.9 Congenital malformation of face and neck, unspecified

Code Version: 2022 ICD-10-CM

Synonyms

• Autosomal recessive facio-digito-genital syndrome
• Bone age finding
• Brachymesophalangia
• Cerebrofacial dysplasia
• Congenital anomaly of anterior portion of neck
• Congenital anomaly of face
• Congenital anomaly of neck
• Congenital cataracts, facial dysmorphism and neuropathy
• Congenital deformity of face
• Congenital fusion of kidneys
• Congenital malformation of eye, ear and neck
• Deafness craniofacial syndrome
• Delayed bone age
• Disorder of ornithine metabolism
• Disturbance of hair cycle
• Dysmorphic facies
• Dysmorphic features
• Ear, face and neck congenital anomalies
• Ear, face and neck congenital anomalies
• Faciocardiorenal syndrome
• Familial visceral neuropathy
• Gingival fibromatosis
• Gingival fibromatosis with facial dysmorphism syndrome
• Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome
• Hereditary gingival fibromatosis
• Heritable disorder of neutrophil function
• Horseshoe kidney
• Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome
• Loose anagen hair syndrome
• Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome
• Megakaryocytic thrombocytopenia
• Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome
• Multiple malformation syndrome, moderate short stature, facial
• Multiple malformation syndrome, moderate short stature, facial
• Multiple malformation syndrome, moderate short stature, facial
• Neurofaciodigitorenal syndrome
• Noonan syndrome-like disorder with loose anagen hair
• Oral-facial-digital syndrome with short stature and brachymesophalangia
• Oro-facial digital syndrome type 9
• Otofaciocervical syndrome
• Otospondylomegaepiphyseal dysplasia
• Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome
• PHIP-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome
• Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome
• Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome
• Short stature with valvular heart disease and characteristic facies syndrome
• Thong Douglas Ferrante syndrome
• TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
• Trichorhinophalangeal syndrome
• Trichorhinophalangeal syndrome type 1 and 3
• Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome
• X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome

Diagnostic Related Group(s)

The code Q18.9 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Minor Skin Disorders With Mcc (606)
• Minor Skin Disorders Without Mcc (607)

References to Index of Diseases and Injuries

The code Q18.9 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital anomaly NOS of face and neck

Crosswalk Information

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

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