Q84.1
BillableCongenital morphological disturbances of hair, NEC
Congenital morphological disturbances of hair, not elsewhere classified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Beaded hair
- Monilethrix
- Pili annulati
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
Related Codes(8)
Q84.0Congenital alopecia
Q84.2Other congenital malformations of hair
Q84.3Anonychia
Q84.4Congenital leukonychia
Q84.5Enlarged and hypertrophic nails
Q84.6Other congenital malformations of nails
Q84.8Other specified congenital malformations of integument
Q84.9Congenital malformation of integument, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(119)
SNOMED CT
- BADS syndrome10170007
- Black locks, oculocutaneous albinism, AND deafness of the sensorineural type10170007
- Pili torti17170005
- Twisted hair17170005
- Trichostasis spinulosa21049007
- Pili annulati21926007
- Ringed hair21926007
- Bayonet hair65950001
- Bjornstad's syndrome67817003
- Björnstad syndrome67817003
- Deafness, pili torti, hypogonadism syndrome67817003
- Hearing loss, pili torti, hypogonadism syndrome67817003
- Pili torti-deafness syndrome67817003
- Beaded hair69488000
- Congenital beaded hair69488000
- Ectodermal dysplasia, syndactyly and pili torti239024004
- CHANDS - Curly hair, ankyloblepharon, nail dysplasia syndrome239037001
- Curly hair, ankyloblepharon, nail dysplasia syndrome239037001
- Congenital woolly hair254231002
- Congenital wooly hair254231002
- Congenital ringed hair254233004
- Autosomal dominant familial woolly hair403794008
- Autosomal dominant familial wooly hair403794008
- Autosomal recessive familial woolly hair403795009
- Autosomal recessive familial wooly hair403795009
- Pili torti with developmental delay and neurological abnormality syndrome716194005
- Carvajal syndrome719835006
- Keratoderma with woolly hair type II719835006
- Keratoderma with wooly hair type II719835006
- Woolly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome719835006
- Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome719835006
- Bork syndrome719910004
- Tricho-retino-dento-digital syndrome719910004
- Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome719910004
- Pili torti onychodysplasia syndrome723451000
- Keratoderma with woolly hair type IV764108000
- Keratoderma with wooly hair type IV764108000
- Woolly hair with palmoplantar keratoderma syndrome764108000
- Wooly hair with palmoplantar keratoderma syndrome764108000
- Skin fragility, wooly hair, palmoplantar keratoderma syndrome778010006
- Skin fragillity, woolly hair, palmoplantar keratoderma syndrome778010006
- Congenital dysplasia of nail unit1142193008
UMLS
- Beaded hairC0546966
- Beaded hair (disorder)C0546966
- Congenital beaded hairC0546966
- Hair, NodoseC0546966
- Hairs, NodoseC0546966
- MonilethricesC0546966
- MonilethrixC0546966
- Nodose HairC0546966
- Nodose HairsC0546966
- beaded hairC0546966
- beading hairC0546966
- hair beadedC0546966
- monilethrixC0546966
- Congenital morphological disturbances of hair, NECC0495628
- Congenital morphological disturbances of hair, not elsewhere classifiedC0495628
- PILI ANNULATIC0263489
- Pili annulatiC0263489
- Pili annulati (disorder)C0263489
- RINGED HAIRC0263489
- Ringed hairC0263489
- annulati piliC0263489
- hair ringC0263489
- ringed hairC0263489
Clinical Terms
- Congenital dysplasia of nail unit
- Keratoderma with wooly hair type II
- Keratoderma with wooly hair type IV
- CHANDS - Curly hair, ankyloblepharon, nail dysplasia syndrome
- Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome
- Pili annulati (disorder)
- Black locks, oculocutaneous albinism, AND deafness of the sensorineural type
- Nodose Hair
- hair beaded
- Autosomal recessive familial woolly hair
- Bjornstad's syndrome
- Beaded hair (disorder)
- Skin fragility, wooly hair, palmoplantar keratoderma syndrome
- Bork syndrome
- Congenital beaded hair
- Nodose Hairs
- beaded hair
- Autosomal dominant familial wooly hair
- ringed hair
- Pili torti with developmental delay and neurological abnormality syndrome
- Björnstad syndrome
- Woolly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome
- Congenital wooly hair
- Monilethrix
- annulati pili
- beading hair
- Pili annulati
- Wooly hair with palmoplantar keratoderma syndrome
- Tricho-retino-dento-digital syndrome
- Hairs, Nodose
- Hair, Nodose
- Monilethrices
- Congenital ringed hair
- hair ring
- Curly hair, ankyloblepharon, nail dysplasia syndrome
- Woolly hair with palmoplantar keratoderma syndrome
- Autosomal recessive familial wooly hair
- Hearing loss, pili torti, hypogonadism syndrome
- Bayonet hair
- Twisted hair
- Carvajal syndrome
- Keratoderma with woolly hair type II
- Pili torti-deafness syndrome
- BADS syndrome
- Congenital woolly hair
- Ectodermal dysplasia, syndactyly and pili torti
- Skin fragillity, woolly hair, palmoplantar keratoderma syndrome
- Trichostasis spinulosa
- Keratoderma with woolly hair type IV
- Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome
- Deafness, pili torti, hypogonadism syndrome
- Pili torti
- Autosomal dominant familial woolly hair
- Pili torti onychodysplasia syndrome
Frequently Asked Questions
What is the ICD-10 code for congenital morphological disturbances of hair, nec?
The ICD-10-CM code for congenital morphological disturbances of hair, nec is Q84.1. The full clinical description is "Congenital morphological disturbances of hair, not elsewhere classified". Q84.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q84.1 mean?
ICD-10-CM code Q84.1 represents “Congenital morphological disturbances of hair, not elsewhere classified”. 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 Q84.1 a billable code?
Yes, Q84.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q84.1 in?
Q84.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q84.1?
Q84.1 has Excludes1 notes indicating codes that cannot be used together with it, including: Menkes' kinky hair syndrome (E83.09).
What SNOMED CT codes does Q84.1 map to?
Q84.1 maps to 20 SNOMED CT concepts: 403794008, 403795009, 10170007, 65950001, 69488000, and 15 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q84.1?
Q84.1 is linked to 3 UMLS Concept Unique Identifiers: C0546966, C0495628, C0263489. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q84.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital morphological disturbances of hair, nec 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 Q84.1?
Q84.1 maps to the ICD-11 code: EC21.0 (Genetic defects of the hair shaft).
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.
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.