Diagnosis Code: 757.39

Short Description: Skin anomaly NEC

Long Description: Other specified anomalies of skin

Code Classification:

• Congenital anomalies (740–759)
  • Congenital anomalies (740-759)
    • 757 Congenital anomalies of the integument
      • 757.39 Skin anomaly NEC

Code Version: 2015 ICD-9-CM

Synonyms

• Acquired perforating pseudoxanthoma elasticum
• Acquired pseudoxanthoma elasticum
• Acral Darier's disease
• Acroerythrokeratoderma
• Acrokeratosis paraneoplastica of Bazex
• Acrokeratosis verruciformis of Darier disease
• Acrokeratosis verruciformis of Hopf
• Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma
• Adult junctional epidermolysis bullosa
• Aplasia cutis congenita
• Aplasia cutis congenita due to teratogenic drug
• Aplasia cutis congenita due to underlying malformation
• Aplasia cutis congenita following intra-uterine infection
• Aplasia cutis congenita in association with epidermolysis bullosa
• Aplasia cutis congenita secondary to malformation syndrome
• Aplasia cutis in Chromosome 4 short-arm deletion syndrome
• Aplasia cutis in Johanson-Blizzard syndrome
• Aplasia cutis in Trisomy 13 syndrome
• Aplasia of skin
• Arteriovenous malformation of skin
• Autosomal dominant epidermolysis bullosa simplex
• Autosomal dominant mutilating keratoderma
• Autosomal dominant pseudoxanthoma elasticum
• Autosomal recessive pseudoxanthoma elasticum
• Bloom syndrome
• Brugsch's syndrome
• Bullous eruption of hand
• Cicatricial junctional epidermolysis bullosa
• Circumscribed palmoplantar keratoderma
• Congenital absence of skin on scalp
• Congenital absence of skin on scalp with epidermal nevi
• Congenital accessory skin tag
• Congenital junctional epidermolysis bullosa
• Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
• Congenital keratoderma
• Congenital palmoplantar and perioral keratoderma of Olmsted
• Congenital scar
• Conjunctivitis associated with epidermolysis bullosa
• Cutaneous lesion resulting from spinal dysraphism
• Cutis verticis gyrata
• Cutis verticis gyrata with acromegaloid phenotype
• Deoxyribonucleic acid instability syndrome
• Diffuse palmoplantar keratoderma of Thost-Unna
• Disorder of apocrine secretion
• Dominant dystrophic epidermolysis bullosa
• Dominant dystrophic epidermolysis bullosa with absence of skin
• Dominant dystrophic epidermolysis bullosa, albopapular type
• Dominant epidermolysis bullosa simplex, Weber-Cockayne type
• Drug-induced epidermolysis bullosa acquisita
• Drug-induced pseudoxanthoma elasticum
• Dyskeratosis congenita
• Dystrophic epidermolysis bullosa
• Dystrophic epidermolysis bullosa inverse type
• Emotional sweating affecting palms and soles
• Epidermolysis bullosa
• Epidermolysis bullosa acquisita, Brunsting-Perry type
• Epidermolysis bullosa acquisita, bullous pemphigoid-like
• Epidermolysis bullosa acquisita, cicatricial pemphigoid-like
• Epidermolysis bullosa acquisita, classical acral type
• Epidermolysis bullosa acquisita, oral mucosal involvement
• Epidermolysis bullosa pruriginosa
• Epidermolysis bullosa simplex
• Epidermolysis bullosa simplex of the hands AND/OR feet
• Epidermolysis bullosa simplex with hypodontia
• Epidermolysis bullosa simplex with mottled pigmentation
• Epidermolysis bullosa simplex with neuromuscular disease
• Epidermolysis bullosa simplex, Ogna type
• Epidermolysis simplex superficialis
• Epidermolytic palmoplantar keratoderma of Vorner
• Erythrokeratoderma
• Erythrokeratoderma progressiva of Gottron
• Familial dyskeratotic comedones
• Flexural Darier's disease
• Focal dermal hypoplasia
• Generalized dystrophic epidermolysis bullosa
• Generalized epidermolysis bullosa simplex
• Generalized junctional epidermolysis bullosa
• Generalized recessive dystrophic epidermolysis bullosa mitis
• Generalized recessive non-mutilating dystrophic epidermolysis bullosa
• Giant porokeratosis
• Goltz syndrome
• Gronblad-Strandberg syndrome
• Hereditary acantholytic dermatosis
• Hereditary benign acanthosis nigricans with insulin resistance
• Hereditary diffuse palmoplantar keratoderma
• Hereditary erythrokeratolysis
• Hereditary follicular keratoses
• Hereditary palmoplantar keratoderma
• Hypertrophic Darier's disease
• Hypotrichosis with keratosis pilaris and lentiginosis
• Hystrix ichthyosis with deafness
• Ichthyosis hystrix
• Ichthyosis hystrix gravior of Rheydt
• Ichthyosis hystrix of Curth-Macklin
• Inherited disorder of keratinization
• Inherited epidermolysis bullosa
• Inherited pseudoxanthoma elasticum
• Inverse junctional epidermolysis bullosa
• Junctional epidermolysis bullosa
• Junctional epidermolysis bullosa gravis of Herlitz
• Junctional epidermolysis bullosa mitis
• Juvenile elastoma
• Keratoderma areata
• Keratoderma due to Dowling-Meara type epidermolysis bullosa simplex
• Keratoderma plantare sulcata
• Keratoderma with deafness
• Keratoderma with mental retardation and spastic paraplegia
• Keratoderma with pachyonychia congenita
• Keratoderma with scleroatrophy of the extremities
• Keratolysis exfoliativa
• Keratosis follicularis
• Keratosis pilaris atrophicans
• Keratosis pilaris decalvans
• Keratosis pilaris with ichthyosis and deafness
• Keratosis rubra pilaris
• Lethal autosomal recessive epidermolysis bullosa simplex
• Lichen spinulosus
• Linear porokeratosis
• Linear/nevoid/zosteriform Darier's disease
• Livedo telangiectatica
• Localized dystrophic epidermolysis bullosa
• Localized junctional epidermolysis bullosa
• Localized recessive dystrophic epidermolysis bullosa
• Lymphedematous keratoderma
• Maleformatio ectodermalis generalisata of Bafverstedt
• Mutilating keratoderma
• Nail dystrophy due to Darier's disease
• Nevus lipomatosus cutaneous superficialis
• Pachydermoperiostosis - familial
• Palmar pitting due to Darier's disease
• Palmoplantar keratoderma transgrediens
• Palmoplantar keratoderma with leukoplakia
• Papuloverrucous palmoplantar keratoderma of Jakac-Wolf
• Porcupine man
• Porokeratosis
• Porokeratosis of Mantoux
• Porokeratosis of Mibelli
• Porokeratosis of Mibelli, linear unilateral type
• Porokeratosis of Mibelli, plaque type
• Porokeratosis of Mibelli, superficial disseminated type
• Pretibial epidermolysis bullosa
• Progressive junctional epidermolysis bullosa
• Progressive palmoplantar keratoderma of Greither
• Progressive recessive dystrophic epidermolysis bullosa
• Pseudoxanthoma elasticum
• Recessive dystrophic epidermolysis bullosa
• Relapsing linear acantholytic dermatosis
• Severe achondrolasia with developmental delay and acanthosis nigricans
• Symmetrical keratoderma
• Xeroderma in genetic syndrome

References to Index of Diseases and Injuries

The code 757.39 has the following ICD-9-CM references to the Index of Diseases and Injuries

• Absence (organ or part) (complete or partial)
  • skin (congenital) 757.39

• Acantholysis 701.8
  • bullosa 757.39

• Acanthosis (acquired) (nigricans) 701.2
  • benign (congenital) 757.39
  • congenital 757.39

• Accessory (congenital)
  • skin tags 757.39

• Acrokeratosis verruciformis 757.39

• Acropachyderma 757.39

• Anomaly, anomalous (congenital) (unspecified type) 759.9
  • skin (appendage) 757.9
    • specified type NEC 757.39
  • specified type NEC
    • skin 757.39

• Aplasia - see also Agenesis
  • skin (congenital) 757.39

• Audry's syndrome (acropachyderma) 757.39

• Bloom (-Machacek) (-Torre) syndrome 757.39

• Brugsch's syndrome (acropachyderma) 757.39

• Chalazoderma 757.39

• Cicatrix (adherent) (contracted) (painful) (vicious) 709.2
  • congenital 757.39

• Cockayne-Weber syndrome (epidermolysis bullosa) 757.39

• Cutis - see also condition
  • verticis gyrata 757.39
    • acquired 701.8

• Darier's disease (congenital) (keratosis follicularis) 757.39
  • due to vitamin A deficiency 264.8
  • meaning erythema annulare centrifugum 695.0

• Dermatolysis (congenital) (exfoliativa) 757.39
  • acquired 701.8
  • eyelids 374.34
  • palpebrarum 374.34
  • senile 701.8

• Disease, diseased - see also Syndrome
  • Darier's (congenital) (keratosis follicularis) 757.39
    • erythema annulare centrifugum 695.0
    • vitamin A deficiency 264.8
  • Goldscheider's (epidermolysis bullosa) 757.39
  • Gougerot-Hailey-Hailey (benign familial chronic pemphigus) 757.39
  • Hailey-Hailey (benign familial chronic pemphigus) 757.39
  • K�bner's (epidermolysis bullosa) 757.39
  • Marie-Bamberger (hypertrophic pulmonary osteoarthropathy) (secondary) 731.2
    • primary or idiopathic (acropachyderma) 757.39
  • Meleda 757.39
  • Mibelli's 757.39
  • Mljet (mal de Meleda) 757.39
  • White's (congenital) (keratosis follicularis) 757.39

• Dyskeratosis (see also Keratosis) 701.1
  • bullosa hereditaria 757.39
  • congenital 757.39
  • follicularis 757.39
    • vitamin A deficiency 264.8

• Elastoma 757.39
  • juvenile 757.39
  • Miescher's (elastosis perforans serpiginosa) 701.1

• Epidermolysis
  • bullosa 757.39

• Friedrich-Erb-Arnold syndrome (acropachyderma) 757.39

• Goldscheider's disease (epidermolysis bullosa) 757.39

• Goltz-Gorlin syndrome (dermal hypoplasia) 757.39

• Gougerot-Hailey-Hailey disease (benign familial chronic pemphigus) 757.39

• Gyrate scalp 757.39

• Hailey-Hailey disease (benign familial chronic pemphigus) 757.39

• Hydromphalus (congenital) (since birth) 757.39

• Hyperkeratosis (see also Keratosis) 701.1
  • congenital 757.39
  • eccentrica 757.39
  • figurata centrifuga atrophica 757.39
  • follicularis 757.39
    • in cutem penetrans 701.1

• Hypoplasia, hypoplasis 759.89
  • dermal, focal (Goltz) 757.39
  • focal dermal 757.39
  • skin 757.39

• Ichthyosis (congenita) 757.1
  • hystrix 757.39
  • palmaris and plantaris 757.39

• Keratoderma, keratodermia (congenital) (palmaris et plantaris) (symmetrical) 757.39
  • acquired 701.1
  • blennorrhagica 701.1
    • gonococcal 098.81
  • climacterium 701.1
  • eccentrica 757.39
  • gonorrheal 098.81
  • punctata 701.1
  • tylodes, progressive 701.1

• Keratolysis exfoliativa (congenital) 757.39
  • acquired 695.89
  • neonatorum 757.39

• Keratoma 701.1
  • congenital 757.39
  • palmaris et plantaris hereditarium 757.39

• Keratosis 701.1
  • congenital (any type) 757.39
  • follicularis 757.39
    • acquired 701.1
    • congenital (acneiformis) (Siemens') 757.39
    • spinulosa (decalvans) 757.39
    • vitamin A deficiency 264.8
  • nigricans 701.2
    • congenital 757.39
  • palmaris et plantaris (symmetrical) 757.39
  • pilaris 757.39
    • acquired 701.1
  • suprafollicularis 757.39
  • vegetans 757.39

• K�bner's disease (epidermolysis bullosa) 757.39

• Lichen 697.9
  • pilaris 757.39
    • acquired 701.1
  • spinulosus 757.39
    • mycotic 117.9

• Mal
  • de Meleda 757.39

• Marie-Bamberger disease or syndrome (hypertrophic) (pulmonary) (secondary) 731.2
  • idiopathic (acropachyderma) 757.39
  • primary (acropachyderma) 757.39

• Megalia, cutis et ossium 757.39

• Mibelli's disease 757.39

• Mljet disease (mal de Meleda) 757.39

• Osteoarthropathy (see also Osteoarthrosis) 715.9
  • chronic idiopathic hypertrophic 757.39
  • familial idiopathic 757.39
  • idiopathic hypertrophic 757.39

• Osteosis
  • acromegaloid 757.39

• Pachydermatocele (congenital) 757.39
  • acquired 701.8

• Pachydermoperiostosis
  • primary idiopathic 757.39

• Pachyperiosteodermia
  • primary or idiopathic 757.39

• Pachyperiostosis
  • primary or idiopathic 757.39

• Particolored infant 757.39

• Pemphigus 694.4
  • benign 694.5
    • chronic familial 757.39
  • congenital, traumatic 757.39

• Pityriasis 696.5
  • pilaris 757.39
    • acquired 701.1
    • Hebra's 696.4

• Porokeratosis 757.39
  • disseminated superficial actinic (DSAP) 692.75

• Pseudoxanthoma elasticum 757.39

• Psorospermosis 136.4
  • follicularis (vegetans) 757.39

• Roy (-Jutras) syndrome (acropachyderma) 757.39

• Sauriderma 757.39

• Scar, scarring (see also Cicatrix) 709.2
  • congenital 757.39

• Siemens' syndrome
  • keratosis follicularis spinulosa (decalvans) 757.39

• Syndrome - see also Disease
  • Audry's (acropachyderma) 757.39
  • Bloom (-Machacek) (-Torre) 757.39
  • Brugsch's (acropachyderma) 757.39
  • Cockayne-Weber (epidermolysis bullosa) 757.39
  • FDH (focal dermal hypoplasia) 757.39
  • Friedrich-Erb-Arnold (acropachyderma) 757.39
  • Goltz-Gorlin (dermal hypoplasia) 757.39
  • Marie's (acromegaly) 253.0
    • primary or idiopathic (acropachyderma) 757.39
  • osteodermopathic hyperostosis 757.39
  • Proteus (dermal hypoplasia) 757.39
  • Roy (-Jutras) (acropachyderma) 757.39
  • Siemens'
    • keratosis follicularis spinulosa (decalvans) 757.39
  • Touraine-Solente-Gol� (acropachyderma) 757.39
  • Uehlinger's (acropachyderma) 757.39
  • Weber-Cockayne (epidermolysis bullosa) 757.39

• Tag (hypertrophied skin) (infected) 701.9
  • skin 701.9
    • accessory 757.39
    • congenital 757.39

• Touraine-Solente-Gol� syndrome (acropachyderma) 757.39

• Tumor (M8000/1) - see also Neoplasm, by site, unspecified nature
  • White-Darier 757.39

• Tylosis 700
  • palmaris et plantaris 757.39

• Uehlinger's syndrome (acropachyderma) 757.39

• Urticaria 708.9
  • perstans hemorrhagica 757.39

• Weber-Cockayne syndrome (epidermolysis bullosa) 757.39

• White's disease (congenital) (keratosis follicularis) 757.39

• Xeroderma (congenital) 757.39
  • acquired 701.1
    • eyelid 373.33
  • eyelid 373.33
  • pigmentosum 757.33
  • vitamin A deficiency 264.8

Crosswalk Information

The code 757.39 converts into the following ICD-10 code(s):

Similar Codes

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

« Previous Code