2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Congential Anomalies 740-759 > Congenital Anomalies Of The Integument 757.* > 2008 ICD-9-CM Diagnosis 757.39 Other specified congenital anomalies of skin  On October 1, 2008 the 2009 ICD-9-CM codes came into effect. Therefore, this code may be out of date. The 2009 version of ICD-9-CM 757.39 can be accessed here. Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties. 757.39 is a specific code that can be used to specify a diagnosis 757.39 contains 119 index entries View the ICD-9-CM Volume 1 757.* hierarchy ICD9Data's sister site ProcedureCodes.com launches with the 2008/09 CPT® codes - read more on the ICD9Data.com blog. 757.39 also known as: Accessory skin tags, congenital Congenital scar Epidermolysis bullosa Keratoderma (congenital) 757.39 excludes: pilonidal cyst (685.0-685.1) Index entries containing 757.39: 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