Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome
Tumour necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
Developmental delay, overweight, facial dysmorphism, behavioural abnormalities syndrome
Congenital anomaly of eye, ear and neck
Bachmann Bupp syndrome
Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome
Gingival fibromatosis with facial dysmorphism syndrome
Hereditary fibrous enlargement of gingiva
Brachymesophalangia
PHIP-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome
Congenital anomaly of face
Chung Jansen syndrome
Dysmorphic features
Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome
Neurofaciodigitorenal syndrome
Congenital malformation of eye, ear and neck
Trichorhinophalangeal syndrome
CCFDN - congenital cataracts, facial dysmorphism and neuropathy
Disorder of ornithine metabolism
Disturbance of hair cycle
Retinitis pigmentosa, deafness, premature ageing, short stature, facial dysmorphism syndrome
CDK13-related disorder
Congenital deformity of neck
Orofaciodigital syndrome with retinal abnormality
Essential tremor
Oral-facial-digital syndrome with short stature and brachymesophalangia
X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome
Noonan syndrome-like disorder with loose anagen hair
Multiple malformation syndrome, moderate short stature, facial with or without genital features
Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome
OFD18 - oral-facial-digital syndrome type 18
Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
Hereditary essential tremor
Autosomal recessive facio-digito-genital syndrome
Megakaryocytic thrombocytopenia
Congenital anomaly of anterior portion of neck
Facial dysmorphism
Deafness craniofacial syndrome
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome
Macrothrombocytopenia, lymphoedema, developmental delay, facial dysmorphism, camptodactyly syndrome
Delayed bone age
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome
Orofaciodigital syndrome type 9
Palatal anomalies, multiple diastemata, facial dysmorphism, developmental delay syndrome
Bone age finding
Facial malformation
Congenital deformity of face
CDK13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome
Oro-facial digital syndrome type 9
Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome
Fusion of kidneys
Ornithine metabolism disorder
Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome
Dysmorphic facies
Congenital anomaly of neck
Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behaviour syndrome
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome
Horseshoe kidney
PHIP-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome
Congenital anomaly NOS of face and neck
Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome
Congenital fusion of kidneys
Facio-digito-genital syndrome Kuwait type
Retarded bone age
Congenital malformation of anterior portion of neck
TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
Trichorhinophalangeal syndrome type I and III
Eastman Bixler syndrome
Hereditary gingival fibromatosis
Takenouchi Kosaki syndrome
Teebi Naguib Alawadi syndrome
Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome
Retinitis pigmentosa, hearing loss, premature ageing, short stature, facial dysmorphism syndrome
Trichorhinophalangeal syndrome type 1 and 3
Oral-facial-digital syndrome type 9
Congenital cataracts, facial dysmorphism and neuropathy
Short stature with valvular heart disease and characteristic facies syndrome
Loose anagen hair syndrome
Familial visceral neuropathy
Heritable disorder of neutrophil function
Cerebrofacial dysplasia
Autosomal recessive faciodigitogenital syndrome
Pleckstrin homology domain interacting protein-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome
Otofaciocervical syndrome
Developmental delay, overweight, facial dysmorphism, behavioral abnormalities syndrome
Aarskog-like syndrome
Congenital malformation of throat
Faciocardiorenal syndrome
Congenital malformation of the neck
Freire Maia Pinheiro Opitz syndrome
Orofaciodigital syndrome type 18
Ornithine decarboxylase deficiency
Thong Douglas Ferrante syndrome
NFDR (neurofaciodigitorenal) syndrome
Fara Chlupackova syndrome
Tosti syndrome
Otospondylomegaepiphyseal dysplasia
Gingival fibromatosis
Multiple malformation syndrome, moderate short stature, facial
Ear, face and neck congenital anomalies

Frequently Asked Questions

What is the ICD-10 code for congenital malformation of face and neck, unspecified?

The ICD-10-CM code for congenital malformation of face and neck, unspecified is Q18.9. The full clinical description is "Congenital malformation of face and neck, unspecified". Q18.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q18.9 mean?

ICD-10-CM code Q18.9 represents “Congenital malformation of face and neck, unspecified”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q18.9 a billable code?

Yes, Q18.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q18.9 in?

Q18.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q18.9?

Q18.9 has Excludes1 notes indicating codes that cannot be used together with it, including: cleft lip and cleft palate (Q35-Q37); conditions classified to Q67.0-Q67.4; congenital malformations of skull and face bones (Q75.-); and 4 more.

What SNOMED CT codes does Q18.9 map to?

Q18.9 maps to 54 SNOMED CT concepts: 725434009, 1222658006, 397651006, 205317004, 702433001, and 49 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q18.9?

Q18.9 is linked to 2 UMLS Concept Unique Identifiers: C2107132, C0869095. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q18.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of face and neck, unspecified affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q18.9?

Q18.9 maps to the ICD-11 code: LD0Z (Structural developmental anomalies primarily affecting one body system, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.