Q18.9
BillableCongenital malformation of face and neck, unspecified
Congenital malformation of face and neck, unspecified
Status
Billable / Specific
Parent Code
Q18Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital anomaly NOS of face and neck
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
- cleft lip and cleft palate (Q35-Q37)
- congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)
- congenital malformation of larynx (Q31.-)
- congenital malformation of lip NEC (Q38.0)
- congenital malformation of nose (Q30.-)
- congenital malformation of parathyroid gland (Q89.2)
- congenital malformation of thyroid gland (Q89.2)
Also Known As / Clinical Terms
SNOMED CT
- Trichorhinophalangeal syndrome18077009
- Familial visceral neuropathy20725005
- Congenital anomaly of neck40052002
- Congenital deformity of neck40052002
- Congenital malformation of the neck40052002
- Horseshoe kidney41729002
- Gingival fibromatosis58569000
- Multiple malformation syndrome, moderate short stature, facial77701002
- Multiple malformation syndrome, moderate short stature, facial with or without genital features77701002
- Cerebrofacial dysplasia109561000
- Hereditary fibrous enlargement of gingiva109620006
- Hereditary gingival fibromatosis109620006
- Delayed bone age123983008
- Retarded bone age123983008
- Ear, face and neck congenital anomalies204223000
- Congenital fusion of kidneys204984002
- Fusion of kidneys204984002
- Brachymesophalangia205317004
- Megakaryocytic thrombocytopenia234483004
- Disorder of ornithine metabolism237928008
- Ornithine metabolism disorder237928008
- Disturbance of hair cycle238734009
- Loose anagen hair syndrome238735005
- Dysmorphic facies248200007
- Congenital anomaly of eye, ear and neck253204009
- Congenital malformation of eye, ear and neck253204009
- Dysmorphic features253978002
- Otospondylomegaepiphyseal dysplasia254060000
- Bone age finding397651006
- Congenital deformity of face398206004
- Congenital anomaly of face398302004
- Facial dysmorphism398302004
- Facial malformation398302004
- Heritable disorder of neutrophil function402794002
- Essential tremor609558009
- Hereditary essential tremor609559001
- CCFDN - congenital cataracts, facial dysmorphism and neuropathy702433001
- Congenital cataracts, facial dysmorphism and neuropathy702433001
- Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome716192009
- Thong Douglas Ferrante syndrome716192009
- Short stature with valvular heart disease and characteristic facies syndrome716193004
- Deafness craniofacial syndrome716245003
- Oral-facial-digital syndrome type 9718680001
- Oro-facial digital syndrome type 9718680001
- Orofaciodigital syndrome type 9718680001
- Orofaciodigital syndrome with retinal abnormality718680001
- Gingival fibromatosis with facial dysmorphism syndrome719687007
- Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome719833004
- Eastman Bixler syndrome723333000
- Faciocardiorenal syndrome723333000
- Noonan syndrome-like disorder with loose anagen hair723444009
- Tosti syndrome723444009
- Aarskog-like syndrome725434009
- Autosomal recessive facio-digito-genital syndrome725434009
- Autosomal recessive faciodigitogenital syndrome725434009
- Facio-digito-genital syndrome Kuwait type725434009
- Teebi Naguib Alawadi syndrome725434009
- Freire Maia Pinheiro Opitz syndrome725908007
- NFDR (neurofaciodigitorenal) syndrome725908007
- Neurofaciodigitorenal syndrome725908007
- Fara Chlupackova syndrome763860004
- Otofaciocervical syndrome763860004
- Congenital anomaly of anterior portion of neck789228000
- Congenital malformation of anterior portion of neck789228000
- Congenital malformation of throat789228000
- Trichorhinophalangeal syndrome type 1 and 3818959006
- Trichorhinophalangeal syndrome type I and III818959006
- X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome1167372000
- Retinitis pigmentosa, deafness, premature ageing, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, hearing loss, premature ageing, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome1172605003
- Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome1172685001
- Macrothrombocytopenia, lymphoedema, developmental delay, facial dysmorphism, camptodactyly syndrome1172685001
- Takenouchi Kosaki syndrome1172685001
- Palatal anomalies, multiple diastemata, facial dysmorphism, developmental delay syndrome1172889005
- Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome1172889005
- OFD18 - oral-facial-digital syndrome type 181177179002
- Oral-facial-digital syndrome with short stature and brachymesophalangia1177179002
- Orofaciodigital syndrome type 181177179002
- Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome1208727002
- Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome1208746001
- Chung Jansen syndrome1208987006
- PHIP-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome1208987006
- PHIP-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome1208987006
- Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome1208987006
- Pleckstrin homology domain interacting protein-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome1208987006
- TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome1208998007
- Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome1208998007
- Tumour necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome1208998007
- Bachmann Bupp syndrome1222658006
- Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome1222658006
- Ornithine decarboxylase deficiency1222658006
- Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome1254650002
- Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome1260130005
- Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behaviour syndrome1260130005
- CDK13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome1299154002
- CDK13-related disorder1299154002
- Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome1299154002
- Developmental delay, overweight, facial dysmorphism, behavioral abnormalities syndrome1340176000
- Developmental delay, overweight, facial dysmorphism, behavioural abnormalities syndrome1340176000
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.
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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.