Congenital anomaly of hair
Taenzer's hair
White forelock
Congenital hypertrichosis
FHEIG syndrome
Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome
Persistent lanugo (disorder)
Keratosis pilaris
Genetic defect of hair shaft
Congenital leuconychia
PIBIDS syndrome, photosensitivity with IBIDS
Trichodysplasia xeroderma syndrome
Isolated anterior cervical hypertrichosis
Curly hair, acral keratoderma, caries syndrome
Fatal infantile diarrhoea with trichorrhexis nodosa
X-linked congenital generalized hypertrichosis
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome
Disturbance of hair cycle
Hair discolouration
Canities
Genetic abnormality of hair shaft
Noonan syndrome-like disorder with loose anagen hair
Congenital hair disorder
Congenital cataract with hypertrichosis and intellectual disability syndrome
Hypertrichosis universalis congenita
Wiedemann Steiner syndrome
Leukonychia totalis, acanthosis-nigricans-like lesions, abnormal hair syndrome
Multiple malformation syndrome, moderate short stature, facial with or without genital features
Osteopathia striata
Hairy throat syndrome
Variation in hair colour
Congenital hypertrichosis (disorder)
Dermotrichic syndrome
Macias-Flores Garcia-Cruz Rivera syndrome
Non-androgenic hypertrichosis with genetic disease
Hypertrichosis, short stature, facial dysmorphism, developmental delay syndrome
Congenital generalized hypertrichosis Macias-Flores type
Sabinas brittle hair syndrome
Hypertrichosis with congenital macrogingivae
Intractable diarrhea with phenotypic anomalies
Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome
CHACS - curly hair, acral keratoderma, caries syndrome
MacDermot Patton Williams syndrome
Oculotrichodysplasia
Trichomegaly with retina pigmentary degeneration and dwarfism syndrome
White forelock with malformations syndrome
Marles-Greenburg-Persaud syndrome
Tricho-hepato-enteric syndrome
Intellectual disability, polydactyly, uncombable hair syndrome
Lanugo
Manitoba oculotrichoanal syndrome
Intractable diarrhoea with phenotypic anomalies
Osteopenia, intellectual disability, sparse hair syndrome
Congenital generalized hypertrichosis
Congenital malformation of hair NOS
Syndromic diarrhea
KP - Keratosis pilaris
Congenital anomaly of hair (disorder)
Hypertrichosis lanuginosa
Marles syndrome
Whyte Murphy syndrome
MOTA - Manitoba oculotrichoanal syndrome
Leukonychia totalis
Fatal infantile diarrhea with trichorrhexis nodosa
CAHMR syndrome
BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome
Tsukahara Kajii syndrome
Amish brittle hair syndrome
Hair defect with photosensitivity and intellectual disability syndrome
Spun glass hair
Phenotypic diarrhoea of infancy
Amaurosis hypertrichosis syndrome
Brittle hair-impaired intellect-decreased fertility-short stature syndrome
Trichothiodystrophy
Malignant down
Congenital generalised hypertrichosis Macias-Flores type
Congenital hypertrichosis lanuginosa
Hypertrichosis congenital
Uncombable hair syndrome
Pili trianguli et canaliculi
Cecatto de Lima Pinheiro syndrome
Congenital leukonychia
CAHMR (cataract, hypertrichosis, mental retardation) syndrome
Congenital hair disorder NOS
Osteopathia striata, pigmentary dermopathy, white forelock syndrome
Syndromic diarrhoea
Trichohepatoenteric syndrome
Keratosis pilaris atrophicans
Trichothiodystrophy type G
Variation in hair color
Onycho-tricho-dysplasia neutropenia syndrome
X-linked congenital generalised hypertrichosis
Hair discoloration
Non-androgenic hypertrichosis co-occurrent and due to genetic disease
Calderón González Cantu syndrome
White forelock with malformations
Ulerythema ophryogenes
Congenital generalised hypertrichosis
Persistent lanugo
Hypertrichosis cubiti
Hairy elbows syndrome
Congenital malformation of hair and hair growth
FHEIG (facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth) syndrome
Oliver McFarlane syndrome
Poliosis
BIDS syndrome
Genetic syndrome with hypermelanosis
Tosti syndrome
Phenotypic diarrhea of infancy
Voorhoeve's disease
Taenzer hair
Kaler Garrity Stern syndrome
Multiple malformation syndrome, moderate short stature, facial
Loose anagen hair syndrome
Kozlowski Krajewska syndrome

Frequently Asked Questions

What is the ICD-10 code for other congenital malformations of hair?

The ICD-10-CM code for other congenital malformations of hair is Q84.2. The full clinical description is "Other congenital malformations of hair". Q84.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q84.2 mean?

ICD-10-CM code Q84.2 represents “Other congenital malformations of hair”. 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 Q84.2 a billable code?

Yes, Q84.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q84.2 in?

Q84.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q84.2 map to?

Q84.2 maps to 53 SNOMED CT concepts: 720983002, 403796005, 1187115008, 722379001, 763686007, and 48 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q84.2?

Q84.2 is linked to 4 UMLS Concept Unique Identifiers: C0265991, C2936812, C0478088, C0265994. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q84.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformations of hair 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 Q84.2?

Q84.2 maps to the ICD-11 code: LC31 (Developmental defects of the nail apparatus).

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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.