Q84.0
BillableCongenital alopecia
Congenital alopecia
Status
Billable / Specific
Parent Code
Q84Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital atrichosis
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Congenital alopecia2965006
- Congenital atrichosis2965006
- Naevoid congenital alopecia2965006
- Nevoid congenital alopecia2965006
- KP - Keratosis pilaris5132005
- Keratosis pilaris5132005
- Acroosteolysis27201004
- Congenital hypotrichia56558005
- Congenital hypotrichosis56558005
- Hypotrichosis congenita56558005
- Cutis laxa, autosomal recessive59451000
- Alopecia universalis86166000
- Universal alopecia areata86166000
- Frontonasal dysplasia sequence86610004
- Median cleft face syndrome86610004
- False anodontia109440005
- Congenital retrognathism109515000
- Retrognathia109515000
- Retrognathism109515000
- Collodion baby205550003
- Lamellar ichthyosis205550003
- Congenital localised alopecia205592008
- Congenital localized alopecia205592008
- Tooth absent234948008
- Tooth missing234948008
- Sclerosing cholangitis235917005
- Odonto-onychial dysplasia with alopecia239019002
- Dwarfism, alopecia, pseudoanodontia, cutis laxa239025003
- ANOTHER (alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy, respiratory tract infection) syndrome239050000
- ANOTHER syndrome239050000
- Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections239050000
- Hypohidrotic ectodermal dysplasia, hypothyroidism, ciliary dyskinesia syndrome239050000
- Cutaneous syndrome with ichthyosis239057002
- Hereditary acroosteolysis254148004
- Congenital alopecia with keratin cysts254225000
- Hypotrichosis with keratosis pilaris and lentiginosis254227008
- Marie Unna congenital hypotrichosis254234005
- Marie Unna hereditary hypotrichosis254234005
- Marie Unna syndrome254234005
- Congenital generalised alopecia268288009
- Congenital generalized alopecia268288009
- Recession of bone298358008
- Vertical alopecia403533001
- Sutural alopecia403534007
- Triangular alopecia403535008
- IFAP - ichthyosis follicularis with alopecia and photophobia403782004
- Ichthyosis follicularis with alopecia and photophobia403782004
- Ichthyosis follicularis with alopecia and photophobia (IFAP)403782004
- Atrichia congenita403798006
- Periodontitis associated with genetic disorder710903001
- Periodontitis co-occurrent with genetic disorder710903001
- Atrichia with papular lesions715963002
- Autosomal recessive palmoplantar keratoderma and congenital alopecia Wallis type719104003
- Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome719104003
- Autosomal dominant palmoplantar keratoderma and congenital alopecia719518004
- Palmoplantar keratoderma and congenital alopecia Stevanovic type719518004
- Taurodontia with absent teeth and sparse hair syndrome719945007
- Alymphoid cystic thymic dysgenesis720345008
- Congenital alopecia and nail dystrophy with severe functional T-cell immunodeficiency720345008
- Pignata Guarino syndrome720345008
- Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome720345008
- T-cell immunodeficiency, congenital alopecia, and nail dystrophy720345008
- Winged helix deficiency720345008
- Choroidal atrophy and alopecia syndrome720850008
- Moloney syndrome720850008
- Regional choroidal atrophy and alopecia720850008
- ACD (alopecia, contracture, dwarfism) mental retardation syndrome720979002
- ACD (alopecia, contracture, dwarfism) syndrome720979002
- Alopecia, contracture, dwarfism, intellectual disability syndrome720979002
- Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome720980004
- Alopecia, psychomotor epilepsy, periodontal pyorrhoea, intellectual disability syndrome720980004
- Shokeir syndrome720980004
- Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome720981000
- Devriendt Vandenberghe Fryns syndrome720981000
- GAPO (growth retardation, alopecia, pseudoanodontia, optic atrophy) syndrome721843003
- GAPO syndrome721843003
- Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome721843003
- HLTRS (hypotrichosis, lymphedema, telangiectasia, renal defect) syndrome723363009
- HLTRS (hypotrichosis, lymphoedema, telangiectasia, renal defect) syndrome723363009
- Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome723363009
- Hypotrichosis, lymphoedema, telangiectasia, renal defect syndrome723363009
- HJMD (hypotrichosis, juvenile macular degeneration) syndrome723364003
- Hypotrichosis with juvenile macular degeneration syndrome723364003
- Hypotrichosis and intellectual disability syndrome Lopes type723365002
- Lopes Marques de Faria syndrome723365002
- MACS (macrocephaly, alopecia, cutis laxa, scoliosis) syndrome723367005
- MACS syndrome723367005
- Macrocephaly, alopecia, cutis laxa, scoliosis syndrome723367005
- RIN2 deficiency723367005
- Tall forehead, sparse hair, skin hyperextensibility, scoliosis syndrome723367005
- Congenital ichthyosis with hypotrichosis syndrome724277002
- Ichthyosis, follicular atrophoderma, hypotrichosis syndrome724277002
- Ichthyosis, hypotrichosis, sclerosing cholangitis syndrome724278007
- NISCH (neonatal ichthyosis, sclerosing cholangitis, hypotrichosis) syndrome724278007
- NISCH syndrome724278007
- Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome724278007
- ALX4 (human aristaless-like 4) related frontonasal dysplasia with alopecia and genital anomaly725029001
- Craniofrontonasal dysplasia with alopecia and hypogonadism725029001
- Frontonasal dysplasia with alopecia and genital abnomality725029001
- Frontonasal dysplasia with alopecia and genital anomaly syndrome725029001
- Developmental anomaly of periodontal tissue737265006
- Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome763404001
- Jagell, Holmgren, Hofer syndrome763404001
- HOPP syndrome763658004
- Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome763658004
- Odonto onycho dysplasia with alopecia syndrome763828007
- Odonto-onycho dysplasia alopecia syndrome763828007
- ANE (alopecia, progressive neurological defect, endocrinopathy) syndrome770941005
- ANE syndrome770941005
- Alopecia, progressive neurological defect, endocrinopathy syndrome770941005
- Sparse hair, short stature, skin anomalies syndrome771182002
- Thumb deformity, alopecia, pigmentation anomaly syndrome771182002
- PARC (poikiloderma, alopecia, retrognathism, cleft palate) syndrome771186004
- PARC syndrome771186004
- Poikiloderma, alopecia, retrognathism, cleft palate syndrome771186004
- Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome773300008
- Whyte syndrome773300008
- SOFT (short stature, onychodysplasia, facial dysmorphism, hypotrichosis) syndrome773625007
- SOFT syndrome773625007
- Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome773625007
- Alopecia, epilepsy, intellectual disability syndrome Moynahan type788417006
- Moynahan syndrome788417006
- Congenital dysplasia of nail unit1142193008
- Absence of teeth1162783002
- MFDA - mandibulofacial dysostosis with alopecia1216943004
- Mandibulofacial dysostosis with alopecia1216943004
UMLS
- ALOPECIA, CONGENITALC0265992
- ALPCC0265992
- Alopecia, congenitalC0265992
- Atrichia congenitaC0265992
- Atrichia congenita (disorder)C0265992
- Congenital AlopeciaC0265992
- Congenital alopeciaC0265992
- Congenital alopecia (disorder)C0265992
- Congenital atrichosisC0265992
- Naevoid congenital alopeciaC0265992
- Nevoid congenital alopeciaC0265992
- atrichia congenitaC0265992
- congenital alopeciaC0265992
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.
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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.