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 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 (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 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 (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 | |