eMedCodes logo

757.39 - Other Specified Anomalies Of Skin

The ICD 9 Code for Other specified anomalies of skin is listed as 757.39.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
ICD 9 CM Field Value
Diagnosis Code: 757.39
Long Description: Other specified anomalies of skin
Short Description: Skin anomaly NEC
Chapter: Congenital Anomalies
Block: Congenital anomalies of the integument (757-757)
Related Descriptions: Acquired perforating pseudoxanthoma elasticum
Acquired pseudoxanthoma elasticum
Acral Darier's disease
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 (Type 7)
Aplasia cutis congenita due to underlying malformation (Type 4)
Aplasia cutis congenita following intra-uterine infection (Type 8)
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6)
Aplasia cutis congenita secondary to malformation syndrome (Type 9)
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
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 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 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 (neurotrophic)
Progressive palmoplantar keratoderma of Greither
Progressive recessive dystrophic epidermolysis bullosa
Pseudoxanthoma elasticum
Recessive dystrophic epidermolysis bullosa
Relapsing linear acantholytic dermatosis
Symmetrical keratoderma
Xeroderma in genetic syndrome
ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD-10-CM Code: Q81.9 - Epidermolysis bullosa, unspecified (approximate)
ICD-10-CM Code: Q82.8 - Other specified congenital malformations of skin (approximate)
ICD-9-CM Siblings (same level / similar specificity) of 757.39:
757.31 - Congenital ectodermal dysplasia
757.32 - Vascular hamartomas
757.33 - Congenital pigmentary anomalies of skin