Diagnosis Code: Q84.0

Short Description: Congenital alopecia

Long Description: Congenital alopecia

The code Q84.0 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Other congenital malformations (Q80-Q89)
    • Other congenital malformations of integument (Q84)
      • Q84.0 Congenital alopecia

Code Version: 2022 ICD-10-CM

Synonyms

• Absence of teeth
• Acroosteolysis
• Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
• Alopecia universalis
• Alopecia, contracture, dwarfism, intellectual disability syndrome
• Alopecia, epilepsy, intellectual disability syndrome Moynahan type
• Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
• Alopecia, progressive neurological defect, endocrinopathy syndrome
• Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome
• Atrichia congenita
• Atrichia with papular lesions
• Autosomal dominant palmoplantar keratoderma and congenital alopecia
• Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome
• Choroidal atrophy and alopecia syndrome
• Congenital alopecia
• Congenital alopecia with keratin cysts
• Congenital generalized alopecia
• Congenital hypotrichia
• Congenital hypotrichia
• Congenital hypotrichia
• Congenital hypotrichia
• Congenital hypotrichia
• Congenital hypotrichia
• Congenital hypotrichia
• Congenital hypotrichia
• Congenital ichthyosis with hypotrichosis syndrome
• Congenital localized alopecia
• Congenital retrognathism
• Cutaneous syndrome with ichthyosis
• Cutis laxa, autosomal recessive
• Developmental anomaly of periodontal tissue
• Dwarfism, alopecia, pseudoanodontia, cutis laxa
• False anodontia
• Frontonasal dysplasia sequence
• Frontonasal dysplasia with alopecia and genital anomaly syndrome
• GAPO syndrome
• Hereditary acroosteolysis
• Hypoplasia of thumb
• Hypotrichosis and intellectual disability syndrome Lopes type
• Hypotrichosis with juvenile macular degeneration syndrome
• Hypotrichosis with keratosis pilaris and lentiginosis
• Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome
• Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome
• Ichthyosis follicularis with alopecia and photophobia
• Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome
• Keratosis pilaris
• Lamellar ichthyosis
• MACS syndrome
• Mandibulofacial dysostosis with alopecia
• Marie Unna syndrome
• Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome
• Odonto onycho dysplasia with alopecia syndrome
• Odonto-onychial dysplasia with alopecia
• Periodontitis co-occurrent with genetic disorder
• Poikiloderma, alopecia, retrognathism, cleft palate syndrome
• Sclerosing cholangitis
• Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome
• Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome
• Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome
• Sutural alopecia
• Taurodontia with absent teeth and sparse hair syndrome
• Thumb deformity, alopecia, pigmentation anomaly syndrome
• Tooth absent
• Triangular alopecia
• Vertical alopecia

Diagnostic Related Group(s)

The code Q84.0 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Minor Skin Disorders With Mcc (606)
• Minor Skin Disorders Without Mcc (607)

References to Index of Diseases and Injuries

The code Q84.0 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital atrichosis

Crosswalk Information

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This page was last updated on: 10/1/2023

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