Diagnosis Code: Q84.2

Short Description: Other congenital malformations of hair

Long Description: Other congenital malformations of hair

The code Q84.2 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)
      • Q84.2 Other congenital malformations of hair

Code Version: 2022 ICD-10-CM

Synonyms

• Amaurosis hypertrichosis syndrome
• Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome
• BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome
• Congenital anomaly of hair
• Congenital cataract with hypertrichosis and intellectual disability syndrome
• Congenital generalized hypertrichosis
• Congenital hypertrichosis
• Congenital hypertrichosis lanuginosa
• Congenital leukonychia
• Curly hair, acral keratoderma, caries syndrome
• Dermotrichic syndrome
• Disturbance of hair cycle
• Genetic defect of hair shaft
• Genetic syndrome with hypermelanosis
• Hair defect with photosensitivity and intellectual disability syndrome
• Hair discoloration
• Hypertrichosis cubiti
• Hypertrichosis lanuginosa
• Hypertrichosis lanuginosa
• Hypertrichosis with congenital macrogingivae
• Intellectual disability, polydactyly, uncombable hair syndrome
• Isolated anterior cervical hypertrichosis
• Keratosis pilaris
• Keratosis pilaris atrophicans
• Lanugo
• Leukonychia totalis
• Leukonychia totalis, acanthosis-nigricans-like lesions, abnormal hair syndrome
• Loose anagen hair syndrome
• Manitoba oculotrichoanal syndrome
• Multiple malformation syndrome, moderate short stature, facial
• Non-androgenic hypertrichosis with genetic disease
• Noonan syndrome-like disorder with loose anagen hair
• Oculotrichodysplasia
• Oliver McFarlane syndrome
• Onycho-tricho-dysplasia neutropenia syndrome
• Osteopathia striata
• Osteopathia striata, pigmentary dermopathy, white forelock syndrome
• Osteopenia, intellectual disability, sparse hair syndrome
• Persistent lanugo
• Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome
• Poliosis
• Sabinas brittle hair syndrome
• Taenzer's hair
• Trichodysplasia xeroderma syndrome
• Trichohepatoenteric syndrome
• Trichothiodystrophy
• Trichothiodystrophy
• Trichothiodystrophy
• Trichothiodystrophy
• Trichothiodystrophy
• Ulerythema ophryogenes
• Uncombable hair syndrome
• Variation in hair color
• White forelock
• White forelock with malformations syndrome
• Wiedemann Steiner syndrome
• X-linked congenital generalized hypertrichosis

Diagnostic Related Group(s)

The code Q84.2 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 Q84.2 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital hypertrichosis
  • Congenital malformation of hair NOS
  • Persistent lanugo

Crosswalk Information

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

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