Congenital misshapen hyoid bone
DNMT3A-related overgrowth syndrome
Eyes wide apart
Bixler Christian Gorlin syndrome
Hemifacial myohyperplasia
Congenital elliptocytosis
Tatton Brown Rahman syndrome
Medial sinus of face and neck
Hypertrichosis, short stature, facial dysmorphism, developmental delay syndrome
DNA methyltransferase 3 alpha overgrowth syndrome
Congenital bent hyoid bone
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
Orbital separation excessive
Congenital hypoplasia of middle third of face
Congenital unilateral hypoplasia of depressor anguli oris
Isolated asymmetric crying facies
Congenital angulated hyoid bone
Congenital bowed hyoid bone
Branchiooculofacial syndrome
Hypertelorism
Synophrys
Tall stature, intellectual disability, facial dysmorphism syndrome
Jugular lymphatic obstruction sequence
Tatton Brown Rahman overgrowth syndrome
Congenital fistula of neck
AMME syndrome
Bencze syndrome
Congenital anomaly of the eyebrow
Fistula colli congenita
Hemifacial hyperplasia
Retrusive midface
Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome
Microphthalmos due to branchio-oculo-facial syndrome
Hereditary ovalocytosis
HMC (hypertelorism, microtia, clefting) syndrome
Short stature, facial and skeletal anomalies, intellectual disability, macrodontia syndrome
Congenital absence of hyoid bone
CLIFAHDD syndrome
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome
Midface retrusion
Medial cyst of face and neck
Double eyebrow
HE - hereditary elliptocytosis
Hemifacial hyperplasia strabismus syndrome
Isolated ACF (asymmetric crying facies)
CHOPS syndrome
Congenital absence of chin
Dyssegmental dysplasia Silverman Handmaker type
Congenital malformation of the eyebrow
Hypertelorism with microtia and facial clefting syndrome
Congenital anomaly of hyoid bone
Congenital small ears
Wiedemann Steiner syndrome
Duplication of eyebrow and syndactyly syndrome
Genetic syndromic childhood obesity
Medial fistula of face and neck
Absent eyebrow
Congenital infiltrating lipomatosis of face
Congenital midfacial hypoplasia
Microtia
Congenital hypoplasia of eyebrow
Developmental malformation of branchial arch
AMME complex
Congenital nephritis
Eyebrow duplication syndactyly syndrome
Eyes widely set
Lambert syndrome
Orbital hypertelorism
CLIFAHDD (congenital limbs, face contractures, hypotonia, developmental delay) syndrome
Hereditary elliptocytosis
Short stature-characteristic facies-mental retardation-macrodontia-skeletal anomalies syndrome
KBG syndrome
Congenital abnormal shape of hyoid bone
Agenesis of hyoid bone
Branchial dysplasia, intellectual disability, inguinal hernia syndrome

Frequently Asked Questions

What is the ICD-10 code for other specified congenital malformations of face and neck?

The ICD-10-CM code for other specified congenital malformations of face and neck is Q18.8. The full clinical description is "Other specified congenital malformations of face and neck". Q18.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q18.8 mean?

ICD-10-CM code Q18.8 represents “Other specified congenital malformations of face and neck”. 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 Q18.8 a billable code?

Yes, Q18.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q18.8 in?

Q18.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q18.8?

Q18.8 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 Q18.8 map to?

Q18.8 maps to 37 SNOMED CT concepts: 720982007, 253208007, 1003576007, 733046006, 721836009, and 32 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q18.8?

Q18.8 is linked to 4 UMLS Concept Unique Identifiers: C1394371, C2910122, C2910123, C0477992. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q18.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified congenital malformations of face and neck 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 Q18.8?

Q18.8 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.