Cutaneous syndrome with ichthyosis
atrichia congenita
Hypohidrotic ectodermal dysplasia, hypothyroidism, ciliary dyskinesia syndrome
GAPO syndrome
Collodion baby
Tooth absent
HOPP syndrome
Keratosis pilaris
GAPO (growth retardation, alopecia, pseudoanodontia, optic atrophy) syndrome
Retrognathia
Frontonasal dysplasia with alopecia and genital abnomality
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome
Odonto-onycho dysplasia alopecia syndrome
Choroidal atrophy and alopecia syndrome
Median cleft face syndrome
SOFT (short stature, onychodysplasia, facial dysmorphism, hypotrichosis) syndrome
Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome
Alopecia, progressive neurological defect, endocrinopathy syndrome
Lopes Marques de Faria syndrome
Acroosteolysis
Cutis laxa, autosomal recessive
HJMD (hypotrichosis, juvenile macular degeneration) syndrome
MACS syndrome
Congenital generalized alopecia
Triangular alopecia
ALPC
Dwarfism, alopecia, pseudoanodontia, cutis laxa
HLTRS (hypotrichosis, lymphoedema, telangiectasia, renal defect) syndrome
Taurodontia with absent teeth and sparse hair syndrome
Marie Unna congenital hypotrichosis
Congenital dysplasia of nail unit
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome
ANOTHER syndrome
Congenital hypotrichosis
PARC syndrome
Congenital atrichosis
Regional choroidal atrophy and alopecia
Universal alopecia areata
NISCH (neonatal ichthyosis, sclerosing cholangitis, hypotrichosis) syndrome
Alopecia, epilepsy, intellectual disability syndrome Moynahan type
Hypotrichosis congenita
ALX4 (human aristaless-like 4) related frontonasal dysplasia with alopecia and genital anomaly
RIN2 deficiency
Congenital alopecia and nail dystrophy with severe functional T-cell immunodeficiency
False anodontia
Ichthyosis follicularis with alopecia and photophobia (IFAP)
Developmental anomaly of periodontal tissue
Frontonasal dysplasia with alopecia and genital anomaly syndrome
MACS (macrocephaly, alopecia, cutis laxa, scoliosis) syndrome
NISCH syndrome
KP - Keratosis pilaris
Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome
Atrichia with papular lesions
Congenital generalised alopecia
Congenital localized alopecia
Tooth missing
Atrichia congenita (disorder)
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
ANE syndrome
Devriendt Vandenberghe Fryns syndrome
Nevoid congenital alopecia
Ichthyosis, hypotrichosis, sclerosing cholangitis syndrome
Odonto onycho dysplasia with alopecia syndrome
IFAP - ichthyosis follicularis with alopecia and photophobia
Recession of bone
Hypotrichosis with keratosis pilaris and lentiginosis
Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome
Congenital hypotrichia
Marie Unna hereditary hypotrichosis
Absence of teeth
Sparse hair, short stature, skin anomalies syndrome
Congenital alopecia (disorder)
Shokeir syndrome
Craniofrontonasal dysplasia with alopecia and hypogonadism
Poikiloderma, alopecia, retrognathism, cleft palate syndrome
Retrognathism
Sclerosing cholangitis
Autosomal dominant palmoplantar keratoderma and congenital alopecia
Vertical alopecia
Alymphoid cystic thymic dysgenesis
MFDA - mandibulofacial dysostosis with alopecia
Marie Unna syndrome
Alopecia universalis
Periodontitis associated with genetic disorder
Thumb deformity, alopecia, pigmentation anomaly syndrome
Winged helix deficiency
Whyte syndrome
ACD (alopecia, contracture, dwarfism) syndrome
Hypotrichosis and intellectual disability syndrome Lopes type
Tall forehead, sparse hair, skin hyperextensibility, scoliosis syndrome
Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome
Pignata Guarino syndrome
Lamellar ichthyosis
Ichthyosis follicularis with alopecia and photophobia
HLTRS (hypotrichosis, lymphedema, telangiectasia, renal defect) syndrome
Naevoid congenital alopecia
Alopecia, psychomotor epilepsy, periodontal pyorrhoea, intellectual disability syndrome
Frontonasal dysplasia sequence
Congenital retrognathism
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome
Hereditary acroosteolysis
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
ANOTHER (alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy, respiratory tract infection) syndrome
PARC (poikiloderma, alopecia, retrognathism, cleft palate) syndrome
Alopecia, congenital
Macrocephaly, alopecia, cutis laxa, scoliosis syndrome
Hypotrichosis, lymphoedema, telangiectasia, renal defect syndrome
Periodontitis co-occurrent with genetic disorder
Moynahan syndrome
Moloney syndrome
Ichthyosis, follicular atrophoderma, hypotrichosis syndrome
Hypotrichosis with juvenile macular degeneration syndrome
SOFT syndrome
Mandibulofacial dysostosis with alopecia
Congenital ichthyosis with hypotrichosis syndrome
Jagell, Holmgren, Hofer syndrome
Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
ANE (alopecia, progressive neurological defect, endocrinopathy) syndrome
Congenital alopecia with keratin cysts
ACD (alopecia, contracture, dwarfism) mental retardation syndrome
Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome
Odonto-onychial dysplasia with alopecia
Palmoplantar keratoderma and congenital alopecia Stevanovic type
Autosomal recessive palmoplantar keratoderma and congenital alopecia Wallis type
Alopecia, contracture, dwarfism, intellectual disability syndrome
Congenital localised alopecia
Sutural alopecia

Frequently Asked Questions

What is the ICD-10 code for congenital alopecia?

The ICD-10-CM code for congenital alopecia is Q84.0. The full clinical description is "Congenital alopecia". Q84.0 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q84.0 mean?

ICD-10-CM code Q84.0 represents “Congenital alopecia”. 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 Q84.0 a billable code?

Yes, Q84.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q84.0 in?

Q84.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q84.0 map to?

Q84.0 maps to 59 SNOMED CT concepts: 720979002, 725029001, 770941005, 239050000, 1162783002, and 54 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q84.0?

Q84.0 is linked to 1 UMLS Concept Unique Identifier: C0265992. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q84.0 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital alopecia 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 Q84.0?

Q84.0 maps to the ICD-11 code: LC30 (Developmental defects of hair or hair growth).

Automate ICD-10 Coding With AI

Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.

Try Free View API Docs

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.