2008 ICD-9-CM Diagnosis Code 757.39 : Other specified congenital anomalies of skin

Free ICD-9-CM Diagnosis Codes > 2008 > Congential Anomalies 740-759 > Congenital anomalies of the integument 757.* >

2008 ICD-9-CM Diagnosis Code 757.39

Other specified congenital anomalies of skin

757.33

757.4

757.39 is a billable ICD-9-CM medical code that can be used to specify a diagnosis on a reimbursement claim.
Newer versions of 757.39: 2009 2010

Diagnosis Definition(s) Click to expand

Excludes

Also applicable to/known as Click to expand

ICD-9-CM Volume 2 Index Entries That Refer To 757.39 Click to expand

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
Köbner'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

Köbner'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-Golé (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-Golé 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

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