ICD-9 Code 757.39
Other specified anomalies of skin
Not Valid for Submission
757.39 is a legacy non-billable code used to specify a medical diagnosis of other specified anomalies of skin. This code was replaced on September 30, 2015 by its ICD-10 equivalent.
ICD-9: | 757.39 |
Short Description: | Skin anomaly NEC |
Long Description: | Other specified anomalies of skin |
Convert 757.39 to ICD-10
The following crosswalk between ICD-9 to ICD-10 is based based on the General Equivalence Mappings (GEMS) information:
Code Classification
-
Congenital anomalies (740–759)
-
Congenital anomalies (740-759)
- 757 Congenital anomalies of the integument
-
Congenital anomalies (740-759)
Information for Medical Professionals
Synonyms
- 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
- 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 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
- Progressive palmoplantar keratoderma of Greither
- Progressive recessive dystrophic epidermolysis bullosa
- Pseudoxanthoma elasticum
- Recessive dystrophic epidermolysis bullosa
- Relapsing linear acantholytic dermatosis
- Severe achondrolasia with developmental delay and acanthosis nigricans
- Symmetrical keratoderma
- Xeroderma in genetic syndrome
Index to Diseases and Injuries
References found for the code 757.39 in the Index of Diseases and Injuries:
- 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
- Aplasia SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. 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 See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. condition- verticis gyrata 757.39
- acquired 701.8
- verticis gyrata 757.39
- 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 See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. 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
- K bner 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
- Darier s congenital keratosis follicularis 757.39
- Dyskeratosis SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. 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 See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. 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
- K bner s disease epidermolysis bullosa 757.39
- Lichen 697.9
- pilaris 757.39
- acquired 701.1
- spinulosus 757.39
- mycotic 117.9
- pilaris 757.39
- 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 See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. 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
- benign 694.5
- Pityriasis 696.5
- pilaris 757.39
- acquired 701.1
- Hebra s 696.4
- pilaris 757.39
- 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 See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Cicatrix 709.2- congenital 757.39
- Siemens syndrome
- keratosis follicularis spinulosa decalvans 757.39
- Syndrome SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. 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 Gol 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
- skin 701.9
- Touraine Solente Gol syndrome acropachyderma 757.39
- Tumor M8000 1 SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. 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
- acquired 701.1
Information for Patients
Skin Conditions
Your skin is your body's largest organ. It covers and protects your body. Your skin:
- Holds body fluids in, preventing dehydration
- Keeps harmful microbes out, preventing infections
- Helps you feel things like heat, cold, and pain
- Keeps your body temperature even
- Makes vitamin D when the sun shines on it
Anything that irritates, clogs, or inflames your skin can cause symptoms such as redness, swelling, burning, and itching. Allergies, irritants, your genetic makeup, and certain diseases and immune system problems can cause rashes, hives, and other skin conditions. Many skin problems, such as acne, also affect your appearance.
NIH: National Institute of Arthritis and Musculoskeletal and Skin Diseases
[Read More]
ICD-9 Footnotes
General Equivalence Map Definitions
The ICD-9 and ICD-10 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.
- Approximate Flag - The approximate flag is on, indicating that the relationship between the code in the source system and the code in the target system is an approximate equivalent.
- No Map Flag - The no map flag indicates that a code in the source system is not linked to any code in the target system.
- Combination Flag - The combination flag indicates that more than one code in the target system is required to satisfy the full equivalent meaning of a code in the source system.
Index of Diseases and Injuries Definitions
- And - The word "and" should be interpreted to mean either "and" or "or" when it appears in a title.
- Code also note - A "code also" note instructs that two codes may be required to fully describe a condition, but this note does not provide sequencing direction.
- Code first - Certain conditions have both an underlying etiology and multiple body system manifestations due to the underlying etiology. For such conditions, the ICD-10-CM has a coding convention that requires the underlying condition be sequenced first followed by the manifestation. Wherever such a combination exists, there is a "use additional code" note at the etiology code, and a "code first" note at the manifestation code. These instructional notes indicate the proper sequencing order of the codes, etiology followed by manifestation.
- Type 1 Excludes Notes - A type 1 Excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- Type 2 Excludes Notes - A type 2 Excludes note represents "Not included here". An excludes2 note indicates that the condition excluded is not part of the condition represented by the code, but a patient may have both conditions at the same time. When an Excludes2 note appears under a code, it is acceptable to use both the code and the excluded code together, when appropriate.
- Includes Notes - This note appears immediately under a three character code title to further define, or give examples of, the content of the category.
- Inclusion terms - List of terms is included under some codes. These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- NEC "Not elsewhere classifiable" - This abbreviation in the Alphabetic Index represents "other specified". When a specific code is not available for a condition, the Alphabetic Index directs the coder to the "other specified” code in the Tabular List.
- NOS "Not otherwise specified" - This abbreviation is the equivalent of unspecified.
- See - The "see" instruction following a main term in the Alphabetic Index indicates that another term should be referenced. It is necessary to go to the main term referenced with the "see" note to locate the correct code.
- See Also - A "see also" instruction following a main term in the Alphabetic Index instructs that there is another main term that may also be referenced that may provide additional Alphabetic Index entries that may be useful. It is not necessary to follow the "see also" note when the original main term provides the necessary code.
- 7th Characters - Certain ICD-10-CM categories have applicable 7th characters. The applicable 7th character is required for all codes within the category, or as the notes in the Tabular List instruct. The 7th character must always be the 7th character in the data field. If a code that requires a 7th character is not 6 characters, a placeholder X must be used to fill in the empty characters.
- With - The word "with" should be interpreted to mean "associated with" or "due to" when it appears in a code title, the Alphabetic Index, or an instructional note in the Tabular List. The word "with" in the Alphabetic Index is sequenced immediately following the main term, not in alphabetical order.