ICD-10 Diagnosis Code Q82.8

Other specified congenital malformations of skin

Diagnosis Code Q82.8

ICD-10: Q82.8
Short Description: Other specified congenital malformations of skin
Long Description: Other specified congenital malformations of skin
This is the 2017 version of the ICD-10-CM diagnosis code Q82.8

Code Classification
  • Congenital malformations, deformations and chromosomal abnormalities
    • Other congenital malformations (Q80-Q89)
      • Other congenital malformations of skin (Q82)

Information for Medical Professionals

Diagnostic Related Groups
The diagnosis code Q82.8 is grouped in the following Diagnostic Related Group(s) (MS-DRG v33.0)


Convert to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 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.

Present on Admission (POA) Additional informationCallout TooltipPresent on Admission
The Present on Admission (POA) indicator is used for diagnosis codes included in claims involving inpatient admissions to general acute care hospitals. POA indicators must be reported to CMS on each claim to facilitate the grouping of diagnoses codes into the proper Diagnostic Related Groups (DRG). CMS publishes a listing of specific diagnosis codes that are exempt from the POA reporting requirement.

The code Q82.8 is exempt from POA reporting.

  • Abnormal dermatoglyphic pattern
  • Abnormal palmar creases
  • Abnormal plantar creases
  • Acquired acanthosis nigricans
  • Acquired perforating pseudoxanthoma elasticum
  • Acquired pseudoxanthoma elasticum
  • Acral Darier's disease
  • Acral peeling skin syndrome
  • Acroerythrokeratoderma
  • Acrokerato-elastoidosis
  • Acrokeratosis
  • Acrokeratosis verruciformis of Darier disease
  • Acrokeratosis verruciformis of Hopf
  • Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma
  • Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
  • Alveolar bone loss
  • Angiomatosis
  • Aplasia cutis congenita secondary to malformation syndrome
  • Atrophoderma
  • Atrophoderma vermiculatum
  • Autosomal dominant dyskeratosis congenita
  • Autosomal dominant mutilating keratoderma
  • Autosomal dominant pseudoxanthoma elasticum
  • Autosomal recessive dyskeratosis congenita
  • Autosomal recessive hypohidrotic ectodermal dysplasia syndrome
  • Autosomal recessive pseudoxanthoma elasticum
  • Benign acanthosis nigricans
  • Bloom syndrome
  • Brugsch's syndrome
  • Chronic anemia
  • Chronic folliculitis
  • Chronic hemolytic anemia
  • Circumscribed palmoplantar keratoderma
  • Congenital absence of skin on scalp
  • Congenital absence of skin on scalp with epidermal nevi
  • Congenital accessory skin tag
  • Congenital cutaneous angiomatosis
  • Congenital deficiency of pigment of skin
  • Congenital dermal sinus
  • Congenital ectodermal defect
  • Congenital fascial dystrophy
  • Congenital hypotrichia
  • Congenital keratoderma
  • Congenital livedo reticularis
  • Congenital melanosis
  • Congenital oculocutaneous hypopigmentation
  • Congenital palmoplantar and perioral keratoderma of Olmsted
  • Congenital scar
  • Congenital skin contracture
  • Congenital/genetic syndrome with poikiloderma
  • Congenital/hereditary cutis laxa
  • Congenital/hereditary hypermelanotic disorder
  • Congenital/hereditary lentiginosis
  • Connective tissue nevus of skin
  • Cutaneous lesion resulting from spina bifida
  • Cutis gyrata syndrome of Beare and Stevenson
  • Cutis laxa
  • Cutis laxa secondary to inherited disorder of connective tissue
  • Cutis laxa with osteodystrophy
  • Cutis laxa, autosomal dominant
  • Cutis laxa, autosomal recessive
  • Cutis laxa, recessive, type I
  • Cutis laxa, recessive, type II
  • Cutis verticis gyrata
  • Dermal connective tissue hamartoma
  • Dermatoglyphs - skin lines
  • Dermatopathia pigmentosa reticularis
  • Dermodental dysplasia
  • Diffuse palmoplantar keratoderma of Thost-Unna
  • Disseminated superficial porokeratosis
  • Dwarfism, alopecia, pseudoanodontia, cutis laxa
  • Dyschromatosis universalis
  • Dyselastosis with cysts and comedones
  • Dyskeratosis congenita
  • Ectodermal dysplasia with tooth-sweating defect
  • Eosinophilic pustular folliculitis
  • Epidermolytic palmoplantar keratoderma of Vorner
  • Erythrokeratoderma
  • Erythrokeratoderma progressiva of Gottron
  • Erythrokeratodermia variabilis
  • Extensive congenital erosions, vesicles and reticulate scarring
  • Familial benign pemphigus
  • Familial focal facial dermal dysplasia
  • Fibrotic disorder of skin
  • Flexural Darier's disease
  • Flynn-Aird syndrome
  • Focal dermal hypoplasia
  • Genodermatosis
  • Giant porokeratosis
  • Goltz syndrome
  • Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification
  • Hemolytic anemia with emphysema AND cutis laxa
  • Hereditary acantholytic dermatosis
  • Hereditary acantholytic dermatosis
  • Hereditary benign acanthosis nigricans
  • Hereditary benign acanthosis nigricans with insulin resistance
  • Hereditary benign intraepithelial dyskeratosis
  • Hereditary clubbing
  • Hereditary diffuse palmoplantar keratoderma
  • Hereditary erythrokeratolysis
  • Hereditary follicular keratoses
  • Hereditary palmoplantar keratoderma
  • Hereditary sclerosing poikiloderma
  • Hereditary sclerosing poikiloderma of Weary
  • Hidrotic ectodermal dysplasia syndrome
  • Howel-Evans' syndrome
  • Hoyeraal-Hreidarsson syndrome
  • Hypertrophic Darier's disease
  • Hypotrichosis with keratosis pilaris and lentiginosis
  • Immunodeficiency associated with chromosomal abnormality
  • Infantile stiff skin syndrome
  • Inherited cutaneous hyperpigmentation
  • Inherited cutis laxa
  • Inherited disorder of keratinization
  • Inherited pseudoxanthoma elasticum
  • Insulin receptor defect
  • Juvenile elastoma
  • Keratoderma
  • Keratoderma areata
  • 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
  • Keratolytic winter erythema
  • Keratosis follicularis
  • Keratosis pilaris
  • Keratosis pilaris atrophicans
  • Keratosis pilaris decalvans
  • Keratosis pilaris with ichthyosis and deafness
  • Keratosis rubra pilaris
  • Kindler's syndrome
  • Kohlschutter's syndrome
  • Lichen spinulosus
  • Linear porokeratosis
  • Linear/nevoid/zosteriform Darier's disease
  • Localized congenital cutis laxa
  • Lumpy scalp syndrome
  • Macrocephaly-capillary malformation
  • Michelin-tire baby
  • Mixed vascular malformation
  • Multiple benign annular creases of extremities
  • Multiple lentigines syndrome
  • Multiple malformation syndrome with senile-like appearance
  • Multiple malformation syndrome, small stature, without skeletal dysplasia
  • Mutilating keratoderma
  • Naegeli-Franceschetti-Jadassohn syndrome
  • Nail dystrophy associated with bullous dermatoses
  • Nail dystrophy due to benign familial pemphigus
  • Nail dystrophy due to Darier's disease
  • Neonatal cutis laxa with marfanoid phenotype
  • Neonatal eosinophilic pustular folliculitis
  • Neonatal skin infection
  • Neurocutaneous melanosis sequence
  • Nevoid lentiginosis
  • Nevus elasticus
  • Oculo-cerebro-cutaneous syndrome
  • Oculodermal melanocytosis
  • Osteodystrophy
  • Palmar pitting due to Darier's disease
  • Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu
  • Palmoplantar keratoderma
  • Palmoplantar keratoderma transgrediens
  • Papillon-Lefèvre syndrome
  • Papuloverrucous palmoplantar keratoderma of Jakac-Wolf
  • Poikiloderma
  • Porokeratosis
  • Porokeratosis of Mantoux
  • Porokeratosis of Mibelli
  • Porokeratosis of Mibelli, linear unilateral type
  • Porokeratosis of Mibelli, plaque type
  • Porokeratosis of Mibelli, superficial disseminated type
  • Preauricular dimple
  • Premature aging syndrome
  • Progressive palmoplantar keratoderma of Greither
  • Pseudoxanthoma elasticum
  • Punctate palmoplantar keratoderma
  • Reticulate pigmented anomaly of flexures
  • Reticulate vascular nevus
  • Rothmund-Thomson syndrome
  • Skin peeling disorder
  • Symmetrical dyschromatosis of extremities
  • Trichodental syndrome
  • Vascular neurocutaneous syndrome
  • Wrinkly skin syndrome
  • X-linked dyskeratosis congenita
  • Zosteriform lentiginosis

Index of Diseases and Injuries
References found for the code Q82.8 in the Index of Diseases and Injuries:

Information for Patients

Skin Conditions

Also called: Cutaneous disorders, Dermatologic disorders

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

  • Acrodermatitis
  • Cradle cap
  • Cryotherapy
  • Cutaneous skin tags
  • Dry skin -- self-care
  • Erythema multiforme
  • Granuloma annulare
  • Keratosis pilaris
  • Lichen planus
  • Milia
  • Sebaceous cyst
  • Seborrheic dermatitis
  • Seborrheic keratosis
  • Skin lesion removal
  • Skin lesion removal-aftercare
  • Stasis dermatitis and ulcers

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