Diagnosis Code: Q82.8

Short Description: Other specified congenital malformations of skin

Long Description: Other specified congenital malformations of skin

The code Q82.8 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Other congenital malformations (Q80-Q89)
    • Other congenital malformations of skin (Q82)
      • Q82.8 Other specified congenital malformations of skin

Code Version: 2022 ICD-10-CM

Synonyms

• Abnormal blue sclerae
• Abnormal dermatoglyphic pattern
• Abnormal palmar creases
• Abnormal plantar creases
• Absence of fingerprints with congenital milia syndrome
• Acanthosis nigricans
• Acanthosis nigricans
• Achondrogenesis
• Achondroplasia
• Acral Darier's disease
• Acral peeling skin syndrome
• Acrocyanosis
• Acroerythrokeratoderma
• Acrokerato-elastoidosis
• Acrokeratosis verruciformis of Darier disease
• Acrokeratosis verruciformis of Hopf
• Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma
• Acroosteolysis
• Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
• Alveolar bone loss
• Ambiguous genitalia
• Angiomatosis
• Aplasia cutis congenita secondary to malformation syndrome
• Arrhythmogenic right ventricular dysplasia
• Autosomal dominant complex hereditary spastic paraplegia
• Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type
• Autosomal dominant dyskeratosis congenita
• Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering
• Autosomal dominant ichthyosis
• Autosomal dominant palmoplantar keratoderma and congenital alopecia
• Autosomal dominant pseudoxanthoma elasticum
• Autosomal recessive cutis laxa type 2A
• Autosomal recessive cutis laxa type 2B
• Autosomal recessive dyskeratosis congenita
• Autosomal recessive familial wooly hair
• Autosomal recessive familial wooly hair
• Autosomal recessive familial wooly hair
• Autosomal recessive hypohidrotic ectodermal dysplasia syndrome
• Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome
• Autosomal recessive pseudoxanthoma elasticum
• Benign acanthosis nigricans
• Bloom syndrome
• Blue nevus of skin
• Brugsch's syndrome
• CAMOS syndrome
• CEDNIK syndrome
• Central cleft lip
• Chronic hemolytic anemia
• Circumscribed palmoplantar keratoderma
• Circumscribed palmoplantar keratoderma
• Clubbing of nail
• Cole disease
• Congenital absence of skin on scalp
• Congenital absence of skin on scalp with epidermal nevi
• Congenital accessory skin tag
• Congenital anomaly of oral mucosa
• Congenital anomaly of oral mucosa
• Congenital anomaly of sclera
• Congenital atrophy of optic nerve
• Congenital clinodactyly
• Congenital clinodactyly of finger
• Congenital clinodactyly of little finger
• Congenital clubnail
• Congenital corneal leukoma
• Congenital cutaneous angiomatosis
• Congenital deficiency of pigment of skin
• Congenital dermal sinus
• Congenital ectodermal defect
• Congenital erosive and vesicular dermatosis
• Congenital extramedullary dermal hematopoiesis
• Congenital hypotrichia
• Congenital keratoderma
• Congenital keratoderma
• Congenital keratoderma
• Congenital lethal erythroderma
• Congenital leukonychia
• Congenital livedo reticularis
• Congenital melanosis
• Congenital oculocutaneous hypopigmentation
• Congenital palmoplantar and perioral keratoderma of Olmsted
• Congenital pigmentary skin anomalies
• Congenital retrognathism
• Congenital scar
• Congenital skin contracture
• Congenital wooly hair
• Congenital wooly hair
• Congenital wooly hair
• Congenital wooly hair
• Connective tissue nevus of skin
• Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome
• Corneal leukoma
• Craniofaciofrontodigital syndrome
• Craniosynostosis, anal anomaly, porokeratosis syndrome
• Curly hair, acral keratoderma, caries syndrome
• 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 with severe pulmonary, gastrointestinal and urinary anomalies
• Cutis laxa, autosomal dominant
• Cutis laxa, autosomal recessive
• Cutis laxa, autosomal recessive
• Cutis laxa, autosomal recessive
• Cutis laxa, recessive, type I
• Cutis laxa, recessive, type II
• Cutis verticis gyrata
• Cutis verticis gyrata
• Cyanosis of skin and/or skin-associated mucous membrane
• Darier disease
• Deaf blind hypopigmentation syndrome Yemenite type
• Dermatitis of the newborn
• Dermatoglyphs - skin lines
• Dermatoleukodystrophy
• Dermatopathia pigmentosa reticularis
• Dermodental dysplasia
• Diffuse dermatitis
• Diffuse palmoplantar keratoderma and acrocyanosis syndrome
• Diffuse palmoplantar keratoderma of Thost-Unna
• Diffuse palmoplantar keratoderma with painful fissures
• Disseminated superficial porokeratosis
• Dwarfism, alopecia, pseudoanodontia, cutis laxa
• Dyschromatosis universalis
• Dyskeratosis congenita
• Dysplasia of larynx
• Eosinophilic pustular folliculitis
• Epidermolytic palmoplantar keratoderma of Vorner
• Erythrokeratoderma
• Erythrokeratoderma progressiva of Gottron
• Erythrokeratodermia cardiomyopathy syndrome
• Erythrokeratodermia variabilis
• Exostosis, anetoderma, brachydactyly type E syndrome
• Extensive congenital erosions, vesicles and reticulate scarring
• Extramedullary hematopoiesis
• Facial dysmorphism, cleft palate, loose skin syndrome
• Familial benign pemphigus
• Familial generalized lentiginosis
• Familial progressive hyper and hypopigmentation
• Fat hypertrophy
• Finding of palmar crease
• Flexural Darier's disease
• Flynn-Aird syndrome
• Focal acral hyperkeratosis
• Focal acral hyperkeratosis
• Focal acral hyperkeratosis
• Focal acral hyperkeratosis
• Focal dermal hypoplasia
• Focal palmoplantar and gingival keratoderma
• Focal palmoplantar keratoderma with joint keratoses
• Frontonasal dysplasia sequence
• Genetic syndrome with hypermelanosis
• Genodermatosis
• Giant porokeratosis
• Hair discoloration
• Hairy malformation of palms and soles
• Hemolytic anemia with emphysema AND cutis laxa
• Hereditary acantholytic dermatosis
• Hereditary acantholytic dermatosis
• Hereditary acantholytic dermatosis
• Hereditary acantholytic dermatosis
• Hereditary acantholytic dermatosis
• Hereditary acantholytic dermatosis
• Hereditary acantholytic dermatosis
• Hereditary acantholytic dermatosis
• Hereditary acantholytic dermatosis
• Hereditary acroosteolysis
• Hereditary benign acanthosis nigricans
• Hereditary benign acanthosis nigricans with insulin resistance
• Hereditary benign intraepithelial dyskeratosis
• Hereditary clubbing
• Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome
• Hereditary diffuse palmoplantar keratoderma
• Hereditary erythrokeratolysis
• Hereditary follicular keratoses
• Hereditary palmoplantar keratoderma
• Hereditary palmoplantar keratoderma Gamborg Nielsen type
• Hereditary sclerosing poikiloderma
• Hereditary sclerosing poikiloderma of Weary
• Hereditary sensorimotor neuropathy with hyperelastic skin
• Hereditary skin peeling syndrome
• Hidrotic ectodermal dysplasia Christianson Fourie type
• Hidrotic ectodermal dysplasia Halal type
• Hidrotic ectodermal dysplasia syndrome
• Howel-Evans' syndrome
• Hoyeraal-Hreidarsson syndrome
• Hyperplasia of gingiva
• Hypertrophic Darier's disease
• Hypohidrosis
• Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome
• Hypoplasia of thumb
• Hypotrichosis with keratosis pilaris and lentiginosis
• Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome
• Inherited cutaneous hyperpigmentation
• Inherited cutis laxa
• Inherited disorder of keratinization
• Inherited pseudoxanthoma elasticum
• Insulin receptor defect
• Isolated congenital adermatoglyphia
• Isolated focal non-epidermolytic palmoplantar keratoderma
• Juvenile elastoma
• Keratoderma
• Keratoderma hereditarium mutilans with ichthyosis syndrome
• Keratolysis exfoliativa
• Keratolytic winter erythema
• Keratosis follicularis, dwarfism, cerebral atrophy syndrome
• Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome
• Keratosis pilaris
• Keratosis pilaris
• Keratosis pilaris atrophicans
• Keratosis pilaris decalvans
• Keratosis rubra pilaris
• Kindler's syndrome
• Kohlschutter's syndrome
• KRT1-related diffuse nonepidermolytic keratoderma
• Leukonychia totalis
• Leukonychia totalis, acanthosis-nigricans-like lesions, abnormal hair syndrome
• Lichen spinulosus
• Linear porokeratosis
• Linear/nevoid/zosteriform Darier's disease
• Lipoma of brain
• Livedo reticularis
• Localized congenital cutis laxa
• Macroencephaly
• MACS syndrome
• Malignant melanoma arising in congenital nevus
• Mass of palm
• MEDNIK syndrome
• Megalencephaly capillary malformation
• Melanin pigmentation of oral mucosa
• Melanosis of mucosa of body orifice
• Michelin-tire baby
• Microphthalmia with linear skin defect syndrome
• Microphthalmos due to Delleman syndrome
• Milia
• Mongolian spot
• Multiple benign annular creases of extremities
• Multiple lentigines syndrome
• Multiple malformation syndrome with senile-like appearance
• Multiple malformation syndrome with senile-like appearance
• Multiple malformation syndrome with senile-like appearance
• Multiple malformation syndrome, small stature, without skeletal dysplasia
• Mutilating keratoderma
• Mutilating keratoderma
• Naegeli-Franceschetti-Jadassohn syndrome
• Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome
• Nail dystrophy due to benign familial pemphigus
• Nail dystrophy due to Darier's disease
• Naxos disease
• Neonatal cutis laxa with marfanoid phenotype
• Neonatal eosinophilic pustular folliculitis
• Neuroectodermal melanolysosomal disease
• Nevus elasticus
• Oculocerebrocutaneous syndrome
• Osteopathia striata
• Osteopathia striata, pigmentary dermopathy, white forelock syndrome
• Osteoporosis and oculocutaneous hypopigmentation syndrome
• Otopalatodigital syndrome spectrum disorder
• Pai syndrome
• Palmar pit
• Palmar pitting due to Darier disease
• Palmoplantar hyperkeratosis sclerodactyly syndrome
• Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu
• Palmoplantar keratoderma
• Palmoplantar keratoderma Nagashima type
• Palmoplantar keratoderma transgrediens
• Palmoplantar keratoderma with clinodactyly syndrome
• Palmoplantar keratoderma with deafness syndrome
• Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome
• Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome
• Palmoplantar keratoderma, spastic paralysis syndrome
• Papillon-Lefèvre syndrome
• Papular epidermal nevi with skyline basal cell layers syndrome
• Papuloverrucous palmoplantar keratoderma of Jakac-Wolf
• Peripheral cyanosis
• Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome
• Poikiloderma, alopecia, retrognathism, cleft palate syndrome
• Porokeratosis
• Porokeratosis of Mibelli
• Porokeratosis plantaris palmaris et disseminata
• Preauricular dimple
• Primary essential cutis verticis gyrata
• Primary non-essential cutis verticis gyrata
• Progressive palmoplantar keratoderma of Greither
• Pseudoxanthoma elasticum
• Punctate palmoplantar keratoderma
• Punctate palmoplantar keratoderma
• Punctate palmoplantar keratoderma
• Punctate palmoplantar keratoderma type 1
• Reticulate pigmented anomaly of flexures
• Rothmund Thomson syndrome type 1
• Rothmund Thomson syndrome type 2
• Rothmund-Thomson syndrome
• SCARF syndrome
• Severe achondroplasia, developmental delay, acanthosis nigricans syndrome
• Severe dermatitis, multiple allergies, metabolic wasting syndrome
• Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome
• Single transverse palmar crease
• Skin fragility, wooly hair, palmoplantar keratoderma syndrome
• Skin peeling disorder
• Skin punctum
• Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome
• Spastic paraplegia, neuropathy, poikiloderma syndrome
• Striate palmoplantar keratoderma
• Symmetrical dyschromatosis of extremities
• Systematized linear porokeratosis
• Talipes cavus
• Terminal osseous dysplasia and pigmentary defect syndrome
• Thumb deformity, alopecia, pigmentation anomaly syndrome
• Torticollis, keloids, cryptorchidism, renal dysplasia syndrome
• Trichodental syndrome
• Trichothiodystrophy
• Variation in hair color
• Vascular neurocutaneous syndrome
• White forelock
• Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome
• Wooly hair with palmoplantar keratoderma syndrome
• Wrinkly skin syndrome
• X-linked dyskeratosis congenita
• Zosteriform lentiginosis

Diagnostic Related Group(s)

The code Q82.8 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Minor Skin Disorders With Mcc (606)
• Minor Skin Disorders Without Mcc (607)

References to Index of Diseases and Injuries

The code Q82.8 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Abnormal palmar creases
  • Accessory skin tags
  • Benign familial pemphigus [Hailey-Hailey]
  • Congenital poikiloderma
  • Cutis laxa (hyperelastica)
  • Dermatoglyphic anomalies
  • Inherited keratosis palmaris et plantaris
  • Keratosis follicularis [Darier-White]
• Type 1 Excludes Notes:
  • Ehlers-Danlos syndromes (@Q79.6*-)

Crosswalk Information

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This page was last updated on: 10/1/2023

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