Q84.2
BillableOther congenital malformations of hair
Other congenital malformations of hair
Status
Billable / Specific
Parent Code
Q84Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital hypertrichosis
- Congenital malformation of hair NOS
- Persistent lanugo
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
- KP - Keratosis pilaris5132005
- Keratosis pilaris5132005
- Variation in hair color12168009
- Variation in hair colour12168009
- Poliosis14240001
- Hypertrichosis lanuginosa25967007
- Malignant down25967007
- Congenital leuconychia47139007
- Congenital leukonychia47139007
- Congenital hypertrichosis56797000
- Hair discoloration59571007
- Hair discolouration59571007
- Congenital anomaly of hair65033000
- Congenital malformation of hair and hair growth65033000
- Multiple malformation syndrome, moderate short stature, facial77701002
- Multiple malformation syndrome, moderate short stature, facial with or without genital features77701002
- Osteopathia striata82663009
- Voorhoeve's disease82663009
- Persistent lanugo90575004
- Taenzer hair205597002
- Taenzer's hair205597002
- Disturbance of hair cycle238734009
- Loose anagen hair syndrome238735005
- Lanugo247524003
- Canities247564004
- White forelock247564004
- Pili trianguli et canaliculi254230001
- Spun glass hair254230001
- Uncombable hair syndrome254230001
- Keratosis pilaris atrophicans400059005
- Ulerythema ophryogenes400126005
- Genetic abnormality of hair shaft402774006
- Genetic defect of hair shaft402774006
- Genetic syndrome with hypermelanosis402780003
- Hypertrichosis with congenital macrogingivae403532006
- PIBIDS syndrome, photosensitivity with IBIDS403781006
- Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome403781006
- Amish brittle hair syndrome403796005
- BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome403796005
- BIDS syndrome403796005
- Brittle hair-impaired intellect-decreased fertility-short stature syndrome403796005
- Congenital hypertrichosis lanuginosa403799003
- Hypertrichosis universalis congenita403799003
- Fatal infantile diarrhea with trichorrhexis nodosa703406006
- Fatal infantile diarrhoea with trichorrhexis nodosa703406006
- Intractable diarrhea with phenotypic anomalies703406006
- Intractable diarrhoea with phenotypic anomalies703406006
- Phenotypic diarrhea of infancy703406006
- Phenotypic diarrhoea of infancy703406006
- Syndromic diarrhea703406006
- Syndromic diarrhoea703406006
- Tricho-hepato-enteric syndrome703406006
- Trichohepatoenteric syndrome703406006
- MOTA - Manitoba oculotrichoanal syndrome703539006
- Manitoba oculotrichoanal syndrome703539006
- Marles syndrome703539006
- Marles-Greenburg-Persaud syndrome703539006
- Hairy throat syndrome717963001
- Isolated anterior cervical hypertrichosis717963001
- Tsukahara Kajii syndrome717963001
- Oliver McFarlane syndrome719944006
- Trichomegaly with retina pigmentary degeneration and dwarfism syndrome719944006
- Amaurosis hypertrichosis syndrome720983002
- Calderón González Cantu syndrome721007005
- Hair defect with photosensitivity and intellectual disability syndrome721007005
- Cecatto de Lima Pinheiro syndrome722062004
- Oculotrichodysplasia722062004
- CAHMR (cataract, hypertrichosis, mental retardation) syndrome722379001
- CAHMR syndrome722379001
- Congenital cataract with hypertrichosis and intellectual disability syndrome722379001
- Noonan syndrome-like disorder with loose anagen hair723444009
- Tosti syndrome723444009
- Trichothiodystrophy723551003
- Kaler Garrity Stern syndrome732954002
- Osteopenia, intellectual disability, sparse hair syndrome732954002
- Non-androgenic hypertrichosis co-occurrent and due to genetic disease733203002
- Non-androgenic hypertrichosis with genetic disease733203002
- Hypertrichosis, short stature, facial dysmorphism, developmental delay syndrome763618001
- Wiedemann Steiner syndrome763618001
- White forelock with malformations763619009
- White forelock with malformations syndrome763619009
- CHACS - curly hair, acral keratoderma, caries syndrome763686007
- Curly hair, acral keratoderma, caries syndrome763686007
- Intellectual disability, polydactyly, uncombable hair syndrome763742008
- Kozlowski Krajewska syndrome763742008
- Leukonychia totalis763792009
- Trichodysplasia xeroderma syndrome766812005
- Hairy elbows syndrome771181009
- Hypertrichosis cubiti771181009
- MacDermot Patton Williams syndrome771181009
- Leukonychia totalis, acanthosis-nigricans-like lesions, abnormal hair syndrome773700005
- Dermotrichic syndrome782916003
- Osteopathia striata, pigmentary dermopathy, white forelock syndrome787408008
- Whyte Murphy syndrome787408008
- Congenital generalised hypertrichosis838368005
- Congenital generalized hypertrichosis838368005
- Onycho-tricho-dysplasia neutropenia syndrome1003381002
- Trichothiodystrophy type G1003381002
- Sabinas brittle hair syndrome1003920007
- Congenital generalised hypertrichosis Macias-Flores type1010628009
- Congenital generalized hypertrichosis Macias-Flores type1010628009
- Macias-Flores Garcia-Cruz Rivera syndrome1010628009
- X-linked congenital generalised hypertrichosis1010628009
- X-linked congenital generalized hypertrichosis1010628009
- Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome1187115008
- FHEIG (facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth) syndrome1304114004
- FHEIG syndrome1304114004
- Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome1304114004
UMLS
- Congenital anomaly of hairC0265991
- Congenital anomaly of hair (disorder)C0265991
- Congenital hair disorderC0265991
- Congenital hair disorder NOSC0265991
- Congenital malformation of hair NOSC0265991
- Congenital malformation of hair and hair growthC0265991
- Congenital hypertrichosisC2936812
- Congenital hypertrichosis (disorder)C2936812
- Hypertrichosis congenitalC2936812
- Other congenital malformations of hairC0478088
- Persistent lanugoC0265994
- Persistent lanugo (disorder)C0265994
Frequently Asked Questions
What is ICD-10 code Q84.2?
ICD-10-CM code Q84.2 represents "Other congenital malformations of hair". It 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.
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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.