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

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2008 ICD-9-CM Diagnosis Code 757.39

Other specified congenital anomalies of skin

Short description: SKIN ANOMALY NEC.
ICD-9-CM 757.39 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 757.39 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
You are viewing the 2008 version of ICD-9-CM 757.39.
More recent version(s) of ICD-9-CM 757.39: 2009 2010 2011 2012 2013 2014 2015.

Convert to ICD-10-CM: 757.39 converts approximately to:

2015/16 ICD-10-CM Q81.9 Epidermolysis bullosa, unspecified
Or:
2015/16 ICD-10-CM Q82.8 Other specified congenital malformations of skin

Approximate Synonyms

Abnl gluteal crease
Abnormal gluteal crease
Accessory skin tag, congenital
Acquired epidermolysis bullosa
Acquired perforating pseudoxanthoma elasticum
Acquired pseudoxanthoma elasticum
Acral Darier's disease
Acroerythrokeratoderma
Acrokeratosis paraneoplastica of Bazex
Acrokeratosis verruciformis
Acrokeratosis verruciformis of Darier disease
Acrokeratosis verruciformis of Hopf
Acrokeratosis verruciforms
ACROKERATOSIS VERRUCIFORMS (disorder)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma
Adult junctional epidermolysis bullosa
Aplasia cutis
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 keratosis follicularis
Congenital keratosis pilaris
Congenital palmoplantar and perioral keratoderma of Olmsted
Congenital scar
Congenital skin contracture
Conjunctivitis associated with epidermolysis bullosa
Cutaneous lesion resulting from spinal dysraphism
Cutis verticis gyrata
Cutis verticis gyrata with acromegaloid phenotype
Darier disease
Dariers disease
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
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 dystrophica
Epidermolysis bullosa letalis
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 benign pemphigus
Familial dyskeratotic comedones
Flegels disease
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 Gorlin syndrome
Goltz syndrome
Goltz-Gorlin (dermal hypoplasia) syndrome
Gronblad-Strandberg syndrome
Hailey disease
Hailey Hailey disease
Hereditary acantholytic dermatosis
Hereditary benign acanthosis nigricans
Hereditary benign acanthosis nigricans with insulin resistance
Hereditary diffuse palmoplantar keratoderma
Hereditary erythrokeratolysis
Hereditary follicular keratoses
Hereditary palmoplantar keratoderma
Howel Evans syndrome
Howel-Evans' syndrome
Hyperkeratosis lenticularis perstans
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
Keratoderma, congenital
Keratolysis exfoliativa
Keratosis follicularis
Keratosis pilaris atrophicans
Keratosis pilaris decalvans
Keratosis pilaris with ichthyosis and deafness
Keratosis pilaris, congenital
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 (skin condition)
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
Proteus syndrome
Pseudoxanthoma elasticum
Recessive dystrophic epidermolysis bullosa
Relapsing linear acantholytic dermatosis
Sacral dimple
Scar, congenital
Symmetrical keratoderma
Xeroderma in genetic syndrome

757.39 Excludes

pilonidal cyst (685.0-685.1)

Applies To

Accessory skin tags, congenital
Congenital scar
Epidermolysis bullosa
Keratoderma (congenital)

ICD-9-CM Volume 2 Index entries containing back-references to 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
  - adrenal (gland) 759.1
  - alimentary tract (complete) (partial) 751.8
    - lower 751.5
    - upper 750.8
  - ankle 755.69
  - anus, anal (canal) 751.5
  - aorta, aortic 747.29
    - arch 747.21
  - appendix 751.5
  - arm 755.59
  - artery (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
    - brain 747.81
    - coronary 746.85
    - eye 743.58
    - pulmonary 747.3
    - retinal 743.58
    - umbilical 747.5
  - auditory canal 744.29
    - causing impairment of hearing 744.02
  - bile duct or passage 751.69
  - bladder 753.8
    - neck 753.8
  - bone(s) 756.9
    - arm 755.59
    - face 756.0
    - leg 755.69
    - pelvic girdle 755.69
    - shoulder girdle 755.59
    - skull 756.0
      - with
        anencephalus 740.0
        encephalocele 742.0
        hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
        microcephalus 742.1
  - brain 742.4
  - breast 757.6
  - broad ligament 752.19
  - bronchus 748.3
  - canal of Nuck 752.89
  - cardiac septal closure 745.8
  - carpus 755.59
  - cartilaginous 756.9
  - cecum 751.5
  - cervix 752.49
  - chest (wall) 756.3
  - chin 744.89
  - ciliary body 743.46
  - circulatory system 747.89
  - clavicle 755.51
  - clitoris 752.49
  - coccyx 756.19
  - colon 751.5
  - common duct 751.69
  - connective tissue 756.89
  - cricoid cartilage 748.3
  - cystic duct 751.69
  - diaphragm 756.6
  - digestive organ(s) or tract 751.8
    - lower 751.5
    - upper 750.8
  - duodenum 751.5
  - ear 744.29
    - auricle 744.29
      - causing impairment of hearing 744.02
    - causing impairment of hearing 744.09
    - inner (causing impairment of hearing) 744.05
    - middle, except ossicles 744.03
      - ossicles 744.04
  - ejaculatory duct 752.89
  - endocrine 759.2
  - epiglottis 748.3
  - esophagus 750.4
  - Eustachian tube 744.24
  - eye 743.8
    - lid 743.63
    - muscle 743.69
  - face 744.89
    - bone(s) 756.0
  - fallopian tube 752.19
  - fascia 756.89
  - femur 755.69
  - fibula 755.69
  - finger 755.59
  - foot 755.67
  - fovea centralis 743.55
  - gallbladder 751.69
  - Gartner's duct 752.89
  - gastrointestinal tract 751.8
  - genitalia, genital organ(s)
    - female 752.89
      - external 752.49
      - internal NEC 752.89
    - male 752.89
      - penis 752.69
      - scrotal transposition 752.81
  - genitourinary tract NEC 752.89
  - glottis 748.3
  - hair 757.4
  - hand 755.59
  - heart 746.89
    - valve NEC 746.89
      - pulmonary 746.09
  - hepatic duct 751.69
  - hydatid of Morgagni 752.89
  - hymen 752.49
  - integument 757.8
  - intestine (large) (small) 751.5
    - fixational type 751.4
  - iris 743.46
  - jejunum 751.5
  - joint 755.8
  - kidney 753.3
  - knee 755.64
  - labium (majus) (minus) 752.49
  - labyrinth, membranous 744.05
  - larynx 748.3
  - leg 755.69
  - lens 743.39
  - limb, except reduction deformity 755.8
    - lower 755.69
      - reduction deformity (see also Deformity, reduction, lower limb) 755.30
    - upper 755.59
      - reduction deformity (see also Deformity, reduction, upper limb) 755.20
  - lip 750.26
  - liver 751.69
  - lung (fissure) (lobe) 748.69
  - meatus urinarius 753.8
  - metacarpus 755.59
  - mouth 750.26
  - muscle 756.89
    - eye 743.69
  - musculoskeletal system, except limbs 756.9
  - nail 757.5
  - neck 744.89
  - nerve 742.8
    - acoustic 742.8
    - optic 742.8
  - nervous system 742.8
  - nipple 757.6
  - nose 748.1
  - organ NEC 759.89
    - of Corti 744.05
  - osseous meatus (ear) 744.03
  - ovary 752.0
  - oviduct 752.19
  - pancreas 751.7
  - parathyroid 759.2
  - patella 755.64
  - pelvic girdle 755.69
  - penis 752.69
  - pericardium 746.89
  - peripheral vascular system NEC (see also Anomaly, peripheral vascular system) 747.60
  - pharynx 750.29
  - pituitary 759.2
  - prostate 752.89
  - radius 755.59
  - rectum 751.5
  - respiratory system 748.8
  - rib 756.3
  - round ligament 752.89
  - sacrum 756.19
  - salivary duct or gland 750.26
  - scapula 755.59
  - sclera 743.47
  - scrotum 752.89
    - transposition 752.81
  - seminal duct or tract 752.89
  - shoulder girdle 755.59
  - site NEC 759.89
  - skin 757.39
  - skull (bone(s)) 756.0
    - with
      - anencephalus 740.0
      - encephalocele 742.0
      - hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
      - microcephalus 742.1
  - specified organ or site NEC 759.89
  - spermatic cord 752.89
  - spinal cord 742.59
  - spine 756.19
  - spleen 759.0
  - sternum 756.3
  - stomach 750.7
  - tarsus 755.67
  - tendon 756.89
  - testis 752.89
  - thorax (wall) 756.3
  - thymus 759.2
  - thyroid (gland) 759.2
    - cartilage 748.3
  - tibia 755.69
  - toe 755.66
  - tongue 750.19
  - trachea (cartilage) 748.3
  - ulna 755.59
  - urachus 753.7
  - ureter 753.4
    - obstructive 753.29
  - urethra 753.8
    - obstructive 753.6
  - urinary tract 753.8
  - uterus 752.3
  - uvula 750.26
  - vagina 752.49
  - vascular NEC (see also Anomaly, peripheral vascular system) 747.60
    - brain 747.81
  - vas deferens 752.89
  - vein(s) (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
    - brain 747.81
    - great 747.49
    - portal 747.49
    - pulmonary 747.49
  - vena cava (inferior) (superior) 747.49
  - vertebra 756.19
  - vulva 752.49
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
  - pulmonary (hypertrophic osteoarthropathy) 731.2
- 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
  - secondary (hypertrophic pulmonary osteoarthropathy) 731.2
- osteodermopathic hyperostosis 757.39
- Proteus (dermal hypoplasia) 757.39
- Roy (-Jutras) (acropachyderma) 757.39
- Siemens'
  - ectodermal dysplasia 757.31
  - 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
  - anus 455.9
  - congenital 757.39
  - preauricular 744.1
  - rectum 455.9
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

757.33

ICD9Data.com

757.4

ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 757.39 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2008 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.

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