757.4 HAIR ANOMALIES NEC


Code Information

Diagnosis Code: 757.4

Short Description: Hair anomalies NEC

Long Description: Specified anomalies of hair

Code Classification:

  • Congenital anomalies (740–759)
    • Congenital anomalies (740-759)
      • 757 Congenital anomalies of the integument
        • 757.4 Hair anomalies NEC

Code Version: 2015 ICD-9-CM


Synonyms

  • Abnormal hair texture
  • Absence of hair - failure to grow
  • Atrichia congenita
  • Autosomal dominant familial woolly hair
  • Autosomal recessive familial woolly hair
  • Bayonet hair
  • Beaded hair
  • Coarse hair
  • Congenital alopecia
  • Congenital alopecia with keratin cysts
  • Congenital generalized alopecia
  • Congenital hypertrichosis
  • Congenital hypertrichosis lanuginosa
  • Congenital hypotrichia
  • Congenital localized alopecia
  • Congenital morphological disturbances of hair
  • Congenital ringed hair
  • Congenital woolly hair
  • Ectodermal dysplasia, syndactyly and pili torti
  • Lanugo
  • Marie Unna syndrome
  • Persistent lanugo
  • Pili annulati
  • Pili torti
  • Taenzer's hair
  • Total congenital alopecia
  • Triangular alopecia
  • Trichoschisis
  • Ulerythema ophryogenes
  • Uncombable hair syndrome
  • Wooly hair

References to Index of Diseases and Injuries

The code 757.4 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Absence (organ or part) (complete or partial)
    • hair (congenital) 757.4
      • acquired - see Alopecia
  • Agenesis - see also Absence, by site, congenital
    • hair 757.4
  • Alopecia (atrophicans) (pregnancy) (premature) (senile) 704.00
    • adnata 757.4
    • congenital, congenitalis 757.4
  • Anomaly, anomalous (congenital) (unspecified type) 759.9
    • hair 757.9
      • specified type NEC 757.4
    • specified type NEC
      • hair 757.4
  • Atrichia, atrichosis 704.00
    • congenital (universal) 757.4
  • Beaded hair (congenital) 757.4
  • Canities (premature) 704.3
    • congenital 757.4
  • Comedones 706.1
    • lanugo 757.4
  • Disease, diseased - see also Syndrome
    • Taenzer's 757.4
  • Grayness, hair (premature) 704.3
    • congenital 757.4
  • Hypertrichosis 704.1
    • congenital 757.4
    • lanuginosa 757.4
      • acquired 704.1
  • Hypoplasia, hypoplasis 759.89
    • hair 757.4
  • Hypotrichosis 704.09
    • congenital 757.4
    • lid (congenital) 757.4
      • acquired 374.55
  • Lanugo (persistent) 757.4
  • Monilethrix (congenital) 757.4
  • Oligotrichia 704.09
    • congenita 757.4
  • Persistence, persistent (congenital) 759.89
    • lanugo 757.4
  • Pili
    • annulati or torti (congenital) 757.4
  • Pinselhaare (congenital) 757.4
  • Poliosis (eyebrow) (eyelashes) 704.3
    • circumscripta (congenital) 757.4
      • acquired 704.3
    • congenital 757.4
  • Ringed hair (congenital) 757.4
  • Taenzer's disease 757.4
  • Thrix annulata (congenital) 757.4
  • Trichostasis spinulosa (congenital) 757.4
  • Twist, twisted
    • hair (congenital) 757.4
  • Ulerythema
    • ophryogenes 757.4
  • Woolly, wooly hair (congenital) (nevus) 757.4

Crosswalk Information

The code 757.4 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
757.4 Right Arrow Q84.0 Congenital alopecia
Q84.1 Congenital morphological disturbances of hair, NEC
Q84.2 Other congenital malformations of hair
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
757.0 Hereditary edema of legs
757.1 Ichthyosis congenita
757.2 Dermatoglyphic anomalies
757.31 Congenital ectodermal dysplasia
757.32 Vascular hamartomas
757.33 Congenital pigmentary anomalies of skin
757.39 Other specified anomalies of skin
757.5 Specified anomalies of nails
757.6 Specified congenital anomalies of breast
757.8 Other specified anomalies of the integument
757.9 Unspecified congenital anomaly of the integument


This page was last updated on: 10/1/2014