Q82.8 Thost-Unna diffuse palmoplantar keratoderma

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Thost-Unna diffuse palmoplantar keratoderma

Thost-Unna diffuse palmoplantar keratoderma
Synonym for Other specified congenital malformations of skin

    Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)|Q80-Q89 Other congenital malformations (Q80-Q89)|Q82 Other congenital malformations of skin

Results for Thost-Unna diffuse palmoplantar keratoderma and additional synonyms


Q82.8
Other specified congenital malformations of skin

Synonyms:

AKV - Acrokeratosis verruciformis|Abnormal dermatoglyphic pattern|Abnormal dermatoglyphic pattern (disorder)|Abnormal palmar creases|Abnormal palmar creases (disorder)|Abnormal plantar creases|Abnormal plantar creases (disorder)|Accessory skin tags|Acne vermoulante|Acquired perforating pseudoxanthoma elasticum|Acquired perforating pseudoxanthoma elasticum (disorder)|Acquired pseudoxanthoma elasticum|Acquired pseudoxanthoma elasticum (disorder)|Acral Darier disease|Acral Darier's disease|Acral Darier's disease (disorder)|Acral peeling skin syndrome|Acral peeling skin syndrome (disorder)|Acroerythrokeratoderma|Acroerythrokeratoderma (disorder)|Acrokerato-elastoidosis|Acrokerato-elastoidosis (disorder)|Acrokeratosis verruciformis of Darier disease|Acrokeratosis verruciformis of Darier disease (disorder)|Acrokeratosis verruciformis of Hopf|Acrokeratosis verruciformis of Hopf (disorder)|Acropachy|Acropigmentation of Dohi|Angiomatosis|Angiomatosis (disorder)|Atrophoderma vermiculatum|Atrophoderma vermiculatum (disorder)|Autosomal dominant dyskeratosis congenita|Autosomal dominant dyskeratosis congenita (disorder)|Autosomal dominant mutilating keratoderma|Autosomal dominant mutilating keratoderma (disorder)|Autosomal dominant pseudoxanthoma elasticum|Autosomal dominant pseudoxanthoma elasticum (disorder)|Autosomal recessive dyskeratosis congenita|Autosomal recessive dyskeratosis congenita (disorder)|Autosomal recessive hypohidrotic ectodermal dysplasia syndrome|Autosomal recessive hypohidrotic ectodermal dysplasia syndrome (disorder)|Autosomal recessive pseudoxanthoma elasticum|Autosomal recessive pseudoxanthoma elasticum (disorder)|BS - Bloom syndrome|Beare-Stevenson cutis gyrata syndrome|Benign acanthosis nigricans|Benign acanthosis nigricans (disorder)|Benign familial chronic pemphigus|Benign familial pemphigus [Hailey-Hailey]|Bloom syndrome|Bloom syndrome (disorder)|Brauer's syndrome|Brugsch syndrome|Brugsch's syndrome|Brugsch's syndrome (disorder)|CMTC - Cutis marmorata telangiectatica congenita|Chalazodermia|Circumscribed palmoplantar keratoderma|Circumscribed palmoplantar keratoderma (disorder)|Clouston syndrome|Cole disease|Cole-Engmann-Zinsser syndrome|Congenital absence of skin on scalp|Congenital absence of skin on scalp (disorder)|Congenital absence of skin on scalp with epidermal naevi|Congenital absence of skin on scalp with epidermal nevi|Congenital absence of skin on scalp with epidermal nevi (disorder)|Congenital accessory skin tag|Congenital accessory skin tag (disorder)|Congenital cutaneous angiomatosis|Congenital cutaneous angiomatosis (disorder)|Congenital deficiency of pigment of skin|Congenital deficiency of pigment of skin (disorder)|Congenital dermal sinus|Congenital dermal sinus (disorder)|Congenital dyskeratosis|Congenital ectodermal defect|Congenital ectodermal defect (disorder)|Congenital fascial dystrophy|Congenital fascial dystrophy (disorder)|Congenital keratoderma|Congenital keratoderma (disorder)|Congenital livedo reticularis|Congenital livedo reticularis (disorder)|Congenital melanosis|Congenital melanosis (disorder)|Congenital oculocutaneous hypopigmentation|Congenital oculocutaneous hypopigmentation (disorder)|Congenital oculodermal melanocytosis|Congenital palmoplantar and perioral keratoderma of Olmsted|Congenital palmoplantar and perioral keratoderma of Olmsted (disorder)|Congenital poikiloderma|Congenital preauricular pit|Congenital scar|Congenital scar (disorder)|Congenital skin contracture|Congenital skin contracture (disorder)|Congenital telangiectatic erythema syndrome|Congenital/genetic syndrome with poikiloderma|Congenital/genetic syndrome with poikiloderma (disorder)|Congenital/hereditary cutis laxa|Congenital/hereditary cutis laxa (disorder)|Congenital/hereditary hypermelanotic disorder|Congenital/hereditary hypermelanotic disorder (disorder)|Cutis gyrata syndrome of Beare and Stevenson|Cutis gyrata syndrome of Beare and Stevenson (disorder)|Cutis laxa|Cutis laxa (disorder)|Cutis laxa (hyperelastica)|Cutis laxa secondary to inherited disorder of connective tissue|Cutis laxa secondary to inherited disorder of connective tissue (disorder)|Cutis laxa with bone dystrophy|Cutis laxa with joint laxity AND retarded development|Cutis laxa with osteodystrophy|Cutis laxa with osteodystrophy (disorder)|Cutis laxa, autosomal dominant|Cutis laxa, autosomal dominant (disorder)|Cutis laxa, autosomal recessive|Cutis laxa, autosomal recessive (disorder)|Cutis laxa, recessive, type I|Cutis laxa, recessive, type I (disorder)|Cutis laxa, recessive, type II|Cutis laxa, recessive, type II (disorder)|Cutis marmorata telangiectasia congenita|Cutis marmorata telangiectatica congenita|Cutis verticis gyrata|Cutis verticis gyrata (disorder)|DKC - Dyskeratosis congenita|DPR - Dermatopathia pigmentosa reticularis|Darier disease|Darier's disease|Darier-White disease|Dermatoglyphic abnormality|Dermatoglyphic anomalies|Dermatoglyphs|Dermatoglyphs - skin lines|Dermatoglyphs - skin lines (disorder)|Dermatolysis|Dermatomegaly|Dermatopathia pigmentosa reticularis|Dermatopathia pigmentosa reticularis (disorder)|Diffuse palmoplantar keratoderma|Diffuse palmoplantar keratoderma of Thost-Unna|Diffuse palmoplantar keratoderma of Thost-Unna (disorder)|Diffuse palmoplantar keratoderma with esophageal cancer|Diffuse palmoplantar keratoderma with oesophageal cancer|Disseminated superficial porokeratosis|Disseminated superficial porokeratosis (disorder)|Dowling-Degos syndrome|Dyschromatosis universalis|Dyschromatosis universalis (disorder)|Dyselastosis with cysts and comedones|Dyselastosis with cysts and comedones (disorder)|Dyskeratosis congenita|Dyskeratosis congenita (disorder)|Dyskeratosis follicularis|Epidermolytic palmoplantar hyperkeratosis|Epidermolytic palmoplantar keratoderma of Vorner|Epidermolytic palmoplantar keratoderma of Vorner (disorder)|Erythrokeratoderma|Erythrokeratoderma (disorder)|Erythrokeratoderma progressiva of Gottron|Erythrokeratoderma progressiva of Gottron (disorder)|Erythrokeratodermia variabilis|Erythrokeratodermia variabilis (disorder)|Erythrokeratolysis hiemalis|Extensive congenital erosions, vesicles and reticulate scarring|Extensive congenital erosions, vesicles and reticulate scarring (disorder)|FDH - Focal dermal hypoplasia|FODH - Focal dermal hypoplasia|Familial benign chronic pemphigus|Familial benign pemphigus|Familial benign pemphigus (disorder)|Familial continual skin peeling|Familial focal facial dermal dysplasia|Familial focal facial dermal dysplasia (disorder)|Flexural Darier disease|Flexural Darier's disease|Flexural Darier's disease (disorder)|Flynn-Aird syndrome|Flynn-Aird syndrome (disorder)|Focal dermal hypoplasia|Focal dermal hypoplasia (disorder)|Focal dermal hypoplasia syndrome|Focal facial dermal dysplasia|Folliculitis ulerythematosa reticulata|Franceschetti-Jadassohn syndrome|Generalised dermatochalasis|Generalised elastolysis|Generalised elastorrhexis|Generalized dermatochalasis|Generalized elastolysis|Generalized elastorrhexis|Genodermatosis|Genodermatosis (disorder)|Giant porokeratosis|Giant porokeratosis (disorder)|Goltz Gorlin syndrome|Goltz syndrome|Goltz syndrome (disorder)|Goltz-Gorlin (dermal hypoplasia) syndrome|Goltz-Gorlin syndrome|Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification|Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification (disorder)|Hailey Hailey disease|Hailey-Hailey disease|Hereditary acropachy|Hereditary benign acanthosis nigricans|Hereditary benign acanthosis nigricans (disorder)|Hereditary benign acanthosis nigricans with insulin resistance|Hereditary benign acanthosis nigricans with insulin resistance (disorder)|Hereditary benign intraepithelial dyskeratosis|Hereditary benign intraepithelial dyskeratosis (disorder)|Hereditary clubbing|Hereditary clubbing (disorder)|Hereditary diffuse palmoplantar keratoderma|Hereditary diffuse palmoplantar keratoderma (disorder)|Hereditary erythrokeratolysis|Hereditary erythrokeratolysis (disorder)|Hereditary follicular keratoses|Hereditary follicular keratoses (disorder)|Hereditary follicular keratosis|Hereditary palmoplantar keratoderma|Hereditary palmoplantar keratoderma (disorder)|Hereditary sclerosing poikiloderma|Hereditary sclerosing poikiloderma (disorder)|Hereditary sclerosing poikiloderma of Weary|Hereditary sclerosing poikiloderma of Weary (disorder)|Hidrotic ectodermal dysplasia|Hidrotic ectodermal dysplasia syndrome|Hidrotic ectodermal dysplasia syndrome (disorder)|Hippocratic fingers|Honeycomb atrophy of face|Howel Evans syndrome|Howel-Evans' syndrome|Howel-Evans' syndrome (disorder)|Howel-Evans-Clark syndrome|Hoyeraal-Hreidarsson syndrome|Hoyeraal-Hreidarsson syndrome (disorder)|Huriez syndrome|Hypertrophic Darier disease|Hypertrophic Darier's disease|Hypertrophic Darier's disease (disorder)|Hypohidrotic autosomal recessive ectodermal dysplasia|Idiopathic deciduous skin|Inherited cutaneous hyperpigmentation|Inherited cutaneous hyperpigmentation (disorder)|Inherited cutis laxa|Inherited cutis laxa (disorder)|Inherited disorder of keratinisation|Inherited disorder of keratinization|Inherited disorder of keratinization (disorder)|Inherited keratosis palmaris et plantaris|Inherited pseudoxanthoma elasticum|Inherited pseudoxanthoma elasticum (disorder)|Insulin receptor defect with insulin-resistant diabetes mellitus and acanthosis nigricans|Insulin-resistant acanthosis nigricans type A|Juvenile elastoma|Juvenile elastoma (disorder)|KP - Keratosis pilaris|Keratoderma|Keratoderma (disorder)|Keratoderma areata|Keratoderma areata (disorder)|Keratoderma plantare sulcata|Keratoderma plantare sulcata (disorder)|Keratoderma striata|Keratoderma with carcinoma of esophagus|Keratoderma with carcinoma of oesophagus|Keratoderma with deafness|Keratoderma with deafness (disorder)|Keratoderma with mental retardation and spastic paraplegia|Keratoderma with mental retardation and spastic paraplegia (disorder)|Keratoderma with pachyonychia congenita|Keratoderma with pachyonychia congenita (disorder)|Keratoderma with scleroatrophy of the extremities|Keratoderma with scleroatrophy of the extremities (disorder)|Keratodermie en aires|Keratolysis exfoliativa|Keratolysis exfoliativa (disorder)|Keratolytic winter erythema|Keratolytic winter erythema (disorder)|Keratosis follicularis|Keratosis follicularis (disorder)|Keratosis follicularis [Darier-White]|Keratosis follicularis spinulosa decalvans|Keratosis pilaris|Keratosis pilaris (disorder)|Keratosis pilaris atrophicans|Keratosis pilaris atrophicans (disorder)|Keratosis pilaris decalvans|Keratosis pilaris decalvans (disorder)|Keratosis pilaris with ichthyosis and deafness|Keratosis pilaris with ichthyosis and deafness (disorder)|Keratosis rubra pilaris|Keratosis rubra pilaris (disorder)|Keratosis spinulosa|Kindler syndrome|Kindler's syndrome|Kindler's syndrome (disorder)|LEOPARD syndrome|Leopard syndrome|Leopard syndrome lentiginosis|Lichen spinulosus|Lichen spinulosus (disorder)|Linear porokeratosis|Linear porokeratosis (disorder)|Linear/nevoid/zosteriform Darier disease|Linear/nevoid/zosteriform Darier's disease|Linear/nevoid/zosteriform Darier's disease (disorder)|Lipomatous hypertrophy|Localised congenital cutis laxa|Localised palmoplantar keratoderma|Localized congenital cutis laxa|Localized congenital cutis laxa (disorder)|Localized palmoplantar keratoderma|Lumpy scalp syndrome|Lumpy scalp syndrome (disorder)|Mal de Meleda|Melanism|Mendes da Costa syndrome|Mibelli's disease|Michelin-tire baby|Michelin-tire baby (disorder)|Michelin-tyre baby|Multiple benign annular creases of extremities|Multiple benign annular creases of extremities (disorder)|Multiple lentigines syndrome|Multiple lentigines syndrome (disorder)|Mutilating keratoderma|Mutilating keratoderma (disorder)|Naegeli's syndrome|Naegeli-Franceschetti-Jadassohn syndrome|Naegeli-Franceschetti-Jadassohn syndrome (disorder)|Naevus fuscocerulophthalmomaxillaris|Naevus of Ota|Nail dystrophy due to Darier disease|Nail dystrophy due to Darier's disease|Nail dystrophy due to Darier's disease (disorder)|Nail dystrophy due to Hailey-Hailey disease|Nail dystrophy due to benign familial pemphigus|Nail dystrophy due to benign familial pemphigus (disorder)|Neonatal cutis laxa with marfanoid phenotype|Neonatal cutis laxa with marfanoid phenotype (disorder)|Neonatal eosinophilic pustular folliculitis|Neonatal eosinophilic pustular folliculitis (disorder)|Neonatal ofuji's disease|Neurocutaneous melanosis sequence|Neurocutaneous melanosis sequence (disorder)|Nevus fuscocerulophthalmomaxillaris|Nevus of Ota|Nodular elastoidosis|Oculodermal melanocytosis|Oculodermal melanocytosis (disorder)|Oudtshoorn disease|PXE - Pseudoxanthoma elasticum|Palmar pitting due to Darier disease|Palmar pitting due to Darier's disease|Palmar pitting due to Darier's disease (disorder)|Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu|Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu (disorder)|Palmoplantar keratoderma|Palmoplantar keratoderma (disorder)|Palmoplantar keratoderma transgrediens|Palmoplantar keratoderma transgrediens (disorder)|Palmoplantar porokeratosis|Papuloverrucous palmoplantar keratoderma of Jakac-Wolf|Papuloverrucous palmoplantar keratoderma of Jakac-Wolf (disorder)|Peeling skin syndrome, acral type|Poikiloderma congenitale|Poikiloderma congenitale syndrome|Polykeratosis of Touraine|Porokeratosis|Porokeratosis (disorder)|Porokeratosis of Mantoux|Porokeratosis of Mantoux (disorder)|Porokeratosis of Mibelli|Porokeratosis of Mibelli (disorder)|Porokeratosis of Mibelli, linear unilateral type|Porokeratosis of Mibelli, linear unilateral type (disorder)|Porokeratosis of Mibelli, plaque type|Porokeratosis of Mibelli, plaque type (disorder)|Porokeratosis of Mibelli, superficial disseminated type|Porokeratosis of Mibelli, superficial disseminated type (disorder)|Preauricular dimple|Preauricular dimple (disorder)|Preauricular pit|Primary elastolysis|Progressive palmoplantar keratoderma|Progressive palmoplantar keratoderma of Greither|Progressive palmoplantar keratoderma of Greither (disorder)|Pseudoacanthosis nigricans|Pseudoxanthoma elasticum|Pseudoxanthoma elasticum (disorder)|Psorospermosis|Psorospermosis follicularis vegetans|Reticulate acropigmentation of Dohi|Reticulate pigmented anomaly of flexures|Reticulate pigmented anomaly of flexures (disorder)|Rothmund-Thomson syndrome|Rothmund-Thomson syndrome (disorder)|Siemens syndrome|Skin lines|Symmetrical dyschromatosis of extremities|Symmetrical dyschromatosis of extremities (disorder)|Symmetrical progressive erythrokeratoderma|Systematised elastorrhexis|Systematized elastorrhexis|Systemic elastorrhexis|Thost-Unna diffuse palmoplantar keratoderma|Thost-Unna keratoderma|Trichodental syndrome|Trichodental syndrome (disorder)|Tylosis|Type 1 aplasia cutis|Type 3 aplasia cutis|Van Lohuizen's syndrome|Vascular neurocutaneous syndrome|Vascular neurocutaneous syndrome (disorder)|Vohwinkel's mutilating keratoderma|WSS - Wrinkly skin syndrome|Weary-Kindler syndrome|Winter erythrokeratolysis|Witkop-Von Sallmann disease|Witkop-von Sallman syndrome|Wrinkly skin syndrome|Wrinkly skin syndrome (disorder)|X-linked dyskeratosis congenita|X-linked dyskeratosis congenita (disorder)|Zinsser-Cole-Engman syndrome|Zinsser-Cole-Engmann syndrome|Zosteriform lentiginosis|Zosteriform lentiginosis (disorder)|Zosteriform porokeratosis

Subcategories:

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    ICD-Search ICD 10 CM (Clinical Modification) 2017 through Healthcare Natural Language Processing & Deep Learning

    ICD-Code / International Statistical Classification of Diseases and Related Health Problems (ICD) for: Thost-Unna diffuse palmoplantar keratoderma

    ICD Code for Disease, Diagnosis Q82.8

    ICD Code an Classification Other specified congenital malformations of skin

    Chapter, Outline, Main Categories, Parent Concepts or Top Concepts: Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)|Q80-Q89 Other congenital malformations (Q80-Q89)|Q82 Other congenital malformations of skin

    Subcategories, subconcepts or child concepts:

    Synonyms:

    Synonyms: Q82.8: Thost-Unna diffuse palmoplantar keratoderma

    Other Synonyms of the Category: AKV - Acrokeratosis verruciformis|Abnormal dermatoglyphic pattern|Abnormal dermatoglyphic pattern (disorder)|Abnormal palmar creases|Abnormal palmar creases (disorder)|Abnormal plantar creases|Abnormal plantar creases (disorder)|Accessory skin tags|Acne vermoulante|Acquired perforating pseudoxanthoma elasticum|Acquired perforating pseudoxanthoma elasticum (disorder)|Acquired pseudoxanthoma elasticum|Acquired pseudoxanthoma elasticum (disorder)|Acral Darier disease|Acral Darier's disease|Acral Darier's disease (disorder)|Acral peeling skin syndrome|Acral peeling skin syndrome (disorder)|Acroerythrokeratoderma|Acroerythrokeratoderma (disorder)|Acrokerato-elastoidosis|Acrokerato-elastoidosis (disorder)|Acrokeratosis verruciformis of Darier disease|Acrokeratosis verruciformis of Darier disease (disorder)|Acrokeratosis verruciformis of Hopf|Acrokeratosis verruciformis of Hopf (disorder)|Acropachy|Acropigmentation of Dohi|Angiomatosis|Angiomatosis (disorder)|Atrophoderma vermiculatum|Atrophoderma vermiculatum (disorder)|Autosomal dominant dyskeratosis congenita|Autosomal dominant dyskeratosis congenita (disorder)|Autosomal dominant mutilating keratoderma|Autosomal dominant mutilating keratoderma (disorder)|Autosomal dominant pseudoxanthoma elasticum|Autosomal dominant pseudoxanthoma elasticum (disorder)|Autosomal recessive dyskeratosis congenita|Autosomal recessive dyskeratosis congenita (disorder)|Autosomal recessive hypohidrotic ectodermal dysplasia syndrome|Autosomal recessive hypohidrotic ectodermal dysplasia syndrome (disorder)|Autosomal recessive pseudoxanthoma elasticum|Autosomal recessive pseudoxanthoma elasticum (disorder)|BS - Bloom syndrome|Beare-Stevenson cutis gyrata syndrome|Benign acanthosis nigricans|Benign acanthosis nigricans (disorder)|Benign familial chronic pemphigus|Benign familial pemphigus [Hailey-Hailey]|Bloom syndrome|Bloom syndrome (disorder)|Brauer's syndrome|Brugsch syndrome|Brugsch's syndrome|Brugsch's syndrome (disorder)|CMTC - Cutis marmorata telangiectatica congenita|Chalazodermia|Circumscribed palmoplantar keratoderma|Circumscribed palmoplantar keratoderma (disorder)|Clouston syndrome|Cole disease|Cole-Engmann-Zinsser syndrome|Congenital absence of skin on scalp|Congenital absence of skin on scalp (disorder)|Congenital absence of skin on scalp with epidermal naevi|Congenital absence of skin on scalp with epidermal nevi|Congenital absence of skin on scalp with epidermal nevi (disorder)|Congenital accessory skin tag|Congenital accessory skin tag (disorder)|Congenital cutaneous angiomatosis|Congenital cutaneous angiomatosis (disorder)|Congenital deficiency of pigment of skin|Congenital deficiency of pigment of skin (disorder)|Congenital dermal sinus|Congenital dermal sinus (disorder)|Congenital dyskeratosis|Congenital ectodermal defect|Congenital ectodermal defect (disorder)|Congenital fascial dystrophy|Congenital fascial dystrophy (disorder)|Congenital keratoderma|Congenital keratoderma (disorder)|Congenital livedo reticularis|Congenital livedo reticularis (disorder)|Congenital melanosis|Congenital melanosis (disorder)|Congenital oculocutaneous hypopigmentation|Congenital oculocutaneous hypopigmentation (disorder)|Congenital oculodermal melanocytosis|Congenital palmoplantar and perioral keratoderma of Olmsted|Congenital palmoplantar and perioral keratoderma of Olmsted (disorder)|Congenital poikiloderma|Congenital preauricular pit|Congenital scar|Congenital scar (disorder)|Congenital skin contracture|Congenital skin contracture (disorder)|Congenital telangiectatic erythema syndrome|Congenital/genetic syndrome with poikiloderma|Congenital/genetic syndrome with poikiloderma (disorder)|Congenital/hereditary cutis laxa|Congenital/hereditary cutis laxa (disorder)|Congenital/hereditary hypermelanotic disorder|Congenital/hereditary hypermelanotic disorder (disorder)|Cutis gyrata syndrome of Beare and Stevenson|Cutis gyrata syndrome of Beare and Stevenson (disorder)|Cutis laxa|Cutis laxa (disorder)|Cutis laxa (hyperelastica)|Cutis laxa secondary to inherited disorder of connective tissue|Cutis laxa secondary to inherited disorder of connective tissue (disorder)|Cutis laxa with bone dystrophy|Cutis laxa with joint laxity AND retarded development|Cutis laxa with osteodystrophy|Cutis laxa with osteodystrophy (disorder)|Cutis laxa, autosomal dominant|Cutis laxa, autosomal dominant (disorder)|Cutis laxa, autosomal recessive|Cutis laxa, autosomal recessive (disorder)|Cutis laxa, recessive, type I|Cutis laxa, recessive, type I (disorder)|Cutis laxa, recessive, type II|Cutis laxa, recessive, type II (disorder)|Cutis marmorata telangiectasia congenita|Cutis marmorata telangiectatica congenita|Cutis verticis gyrata|Cutis verticis gyrata (disorder)|DKC - Dyskeratosis congenita|DPR - Dermatopathia pigmentosa reticularis|Darier disease|Darier's disease|Darier-White disease|Dermatoglyphic abnormality|Dermatoglyphic anomalies|Dermatoglyphs|Dermatoglyphs - skin lines|Dermatoglyphs - skin lines (disorder)|Dermatolysis|Dermatomegaly|Dermatopathia pigmentosa reticularis|Dermatopathia pigmentosa reticularis (disorder)|Diffuse palmoplantar keratoderma|Diffuse palmoplantar keratoderma of Thost-Unna|Diffuse palmoplantar keratoderma of Thost-Unna (disorder)|Diffuse palmoplantar keratoderma with esophageal cancer|Diffuse palmoplantar keratoderma with oesophageal cancer|Disseminated superficial porokeratosis|Disseminated superficial porokeratosis (disorder)|Dowling-Degos syndrome|Dyschromatosis universalis|Dyschromatosis universalis (disorder)|Dyselastosis with cysts and comedones|Dyselastosis with cysts and comedones (disorder)|Dyskeratosis congenita|Dyskeratosis congenita (disorder)|Dyskeratosis follicularis|Epidermolytic palmoplantar hyperkeratosis|Epidermolytic palmoplantar keratoderma of Vorner|Epidermolytic palmoplantar keratoderma of Vorner (disorder)|Erythrokeratoderma|Erythrokeratoderma (disorder)|Erythrokeratoderma progressiva of Gottron|Erythrokeratoderma progressiva of Gottron (disorder)|Erythrokeratodermia variabilis|Erythrokeratodermia variabilis (disorder)|Erythrokeratolysis hiemalis|Extensive congenital erosions, vesicles and reticulate scarring|Extensive congenital erosions, vesicles and reticulate scarring (disorder)|FDH - Focal dermal hypoplasia|FODH - Focal dermal hypoplasia|Familial benign chronic pemphigus|Familial benign pemphigus|Familial benign pemphigus (disorder)|Familial continual skin peeling|Familial focal facial dermal dysplasia|Familial focal facial dermal dysplasia (disorder)|Flexural Darier disease|Flexural Darier's disease|Flexural Darier's disease (disorder)|Flynn-Aird syndrome|Flynn-Aird syndrome (disorder)|Focal dermal hypoplasia|Focal dermal hypoplasia (disorder)|Focal dermal hypoplasia syndrome|Focal facial dermal dysplasia|Folliculitis ulerythematosa reticulata|Franceschetti-Jadassohn syndrome|Generalised dermatochalasis|Generalised elastolysis|Generalised elastorrhexis|Generalized dermatochalasis|Generalized elastolysis|Generalized elastorrhexis|Genodermatosis|Genodermatosis (disorder)|Giant porokeratosis|Giant porokeratosis (disorder)|Goltz Gorlin syndrome|Goltz syndrome|Goltz syndrome (disorder)|Goltz-Gorlin (dermal hypoplasia) syndrome|Goltz-Gorlin syndrome|Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification|Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification (disorder)|Hailey Hailey disease|Hailey-Hailey disease|Hereditary acropachy|Hereditary benign acanthosis nigricans|Hereditary benign acanthosis nigricans (disorder)|Hereditary benign acanthosis nigricans with insulin resistance|Hereditary benign acanthosis nigricans with insulin resistance (disorder)|Hereditary benign intraepithelial dyskeratosis|Hereditary benign intraepithelial dyskeratosis (disorder)|Hereditary clubbing|Hereditary clubbing (disorder)|Hereditary diffuse palmoplantar keratoderma|Hereditary diffuse palmoplantar keratoderma (disorder)|Hereditary erythrokeratolysis|Hereditary erythrokeratolysis (disorder)|Hereditary follicular keratoses|Hereditary follicular keratoses (disorder)|Hereditary follicular keratosis|Hereditary palmoplantar keratoderma|Hereditary palmoplantar keratoderma (disorder)|Hereditary sclerosing poikiloderma|Hereditary sclerosing poikiloderma (disorder)|Hereditary sclerosing poikiloderma of Weary|Hereditary sclerosing poikiloderma of Weary (disorder)|Hidrotic ectodermal dysplasia|Hidrotic ectodermal dysplasia syndrome|Hidrotic ectodermal dysplasia syndrome (disorder)|Hippocratic fingers|Honeycomb atrophy of face|Howel Evans syndrome|Howel-Evans' syndrome|Howel-Evans' syndrome (disorder)|Howel-Evans-Clark syndrome|Hoyeraal-Hreidarsson syndrome|Hoyeraal-Hreidarsson syndrome (disorder)|Huriez syndrome|Hypertrophic Darier disease|Hypertrophic Darier's disease|Hypertrophic Darier's disease (disorder)|Hypohidrotic autosomal recessive ectodermal dysplasia|Idiopathic deciduous skin|Inherited cutaneous hyperpigmentation|Inherited cutaneous hyperpigmentation (disorder)|Inherited cutis laxa|Inherited cutis laxa (disorder)|Inherited disorder of keratinisation|Inherited disorder of keratinization|Inherited disorder of keratinization (disorder)|Inherited keratosis palmaris et plantaris|Inherited pseudoxanthoma elasticum|Inherited pseudoxanthoma elasticum (disorder)|Insulin receptor defect with insulin-resistant diabetes mellitus and acanthosis nigricans|Insulin-resistant acanthosis nigricans type A|Juvenile elastoma|Juvenile elastoma (disorder)|KP - Keratosis pilaris|Keratoderma|Keratoderma (disorder)|Keratoderma areata|Keratoderma areata (disorder)|Keratoderma plantare sulcata|Keratoderma plantare sulcata (disorder)|Keratoderma striata|Keratoderma with carcinoma of esophagus|Keratoderma with carcinoma of oesophagus|Keratoderma with deafness|Keratoderma with deafness (disorder)|Keratoderma with mental retardation and spastic paraplegia|Keratoderma with mental retardation and spastic paraplegia (disorder)|Keratoderma with pachyonychia congenita|Keratoderma with pachyonychia congenita (disorder)|Keratoderma with scleroatrophy of the extremities|Keratoderma with scleroatrophy of the extremities (disorder)|Keratodermie en aires|Keratolysis exfoliativa|Keratolysis exfoliativa (disorder)|Keratolytic winter erythema|Keratolytic winter erythema (disorder)|Keratosis follicularis|Keratosis follicularis (disorder)|Keratosis follicularis [Darier-White]|Keratosis follicularis spinulosa decalvans|Keratosis pilaris|Keratosis pilaris (disorder)|Keratosis pilaris atrophicans|Keratosis pilaris atrophicans (disorder)|Keratosis pilaris decalvans|Keratosis pilaris decalvans (disorder)|Keratosis pilaris with ichthyosis and deafness|Keratosis pilaris with ichthyosis and deafness (disorder)|Keratosis rubra pilaris|Keratosis rubra pilaris (disorder)|Keratosis spinulosa|Kindler syndrome|Kindler's syndrome|Kindler's syndrome (disorder)|LEOPARD syndrome|Leopard syndrome|Leopard syndrome lentiginosis|Lichen spinulosus|Lichen spinulosus (disorder)|Linear porokeratosis|Linear porokeratosis (disorder)|Linear/nevoid/zosteriform Darier disease|Linear/nevoid/zosteriform Darier's disease|Linear/nevoid/zosteriform Darier's disease (disorder)|Lipomatous hypertrophy|Localised congenital cutis laxa|Localised palmoplantar keratoderma|Localized congenital cutis laxa|Localized congenital cutis laxa (disorder)|Localized palmoplantar keratoderma|Lumpy scalp syndrome|Lumpy scalp syndrome (disorder)|Mal de Meleda|Melanism|Mendes da Costa syndrome|Mibelli's disease|Michelin-tire baby|Michelin-tire baby (disorder)|Michelin-tyre baby|Multiple benign annular creases of extremities|Multiple benign annular creases of extremities (disorder)|Multiple lentigines syndrome|Multiple lentigines syndrome (disorder)|Mutilating keratoderma|Mutilating keratoderma (disorder)|Naegeli's syndrome|Naegeli-Franceschetti-Jadassohn syndrome|Naegeli-Franceschetti-Jadassohn syndrome (disorder)|Naevus fuscocerulophthalmomaxillaris|Naevus of Ota|Nail dystrophy due to Darier disease|Nail dystrophy due to Darier's disease|Nail dystrophy due to Darier's disease (disorder)|Nail dystrophy due to Hailey-Hailey disease|Nail dystrophy due to benign familial pemphigus|Nail dystrophy due to benign familial pemphigus (disorder)|Neonatal cutis laxa with marfanoid phenotype|Neonatal cutis laxa with marfanoid phenotype (disorder)|Neonatal eosinophilic pustular folliculitis|Neonatal eosinophilic pustular folliculitis (disorder)|Neonatal ofuji's disease|Neurocutaneous melanosis sequence|Neurocutaneous melanosis sequence (disorder)|Nevus fuscocerulophthalmomaxillaris|Nevus of Ota|Nodular elastoidosis|Oculodermal melanocytosis|Oculodermal melanocytosis (disorder)|Oudtshoorn disease|PXE - Pseudoxanthoma elasticum|Palmar pitting due to Darier disease|Palmar pitting due to Darier's disease|Palmar pitting due to Darier's disease (disorder)|Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu|Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu (disorder)|Palmoplantar keratoderma|Palmoplantar keratoderma (disorder)|Palmoplantar keratoderma transgrediens|Palmoplantar keratoderma transgrediens (disorder)|Palmoplantar porokeratosis|Papuloverrucous palmoplantar keratoderma of Jakac-Wolf|Papuloverrucous palmoplantar keratoderma of Jakac-Wolf (disorder)|Peeling skin syndrome, acral type|Poikiloderma congenitale|Poikiloderma congenitale syndrome|Polykeratosis of Touraine|Porokeratosis|Porokeratosis (disorder)|Porokeratosis of Mantoux|Porokeratosis of Mantoux (disorder)|Porokeratosis of Mibelli|Porokeratosis of Mibelli (disorder)|Porokeratosis of Mibelli, linear unilateral type|Porokeratosis of Mibelli, linear unilateral type (disorder)|Porokeratosis of Mibelli, plaque type|Porokeratosis of Mibelli, plaque type (disorder)|Porokeratosis of Mibelli, superficial disseminated type|Porokeratosis of Mibelli, superficial disseminated type (disorder)|Preauricular dimple|Preauricular dimple (disorder)|Preauricular pit|Primary elastolysis|Progressive palmoplantar keratoderma|Progressive palmoplantar keratoderma of Greither|Progressive palmoplantar keratoderma of Greither (disorder)|Pseudoacanthosis nigricans|Pseudoxanthoma elasticum|Pseudoxanthoma elasticum (disorder)|Psorospermosis|Psorospermosis follicularis vegetans|Reticulate acropigmentation of Dohi|Reticulate pigmented anomaly of flexures|Reticulate pigmented anomaly of flexures (disorder)|Rothmund-Thomson syndrome|Rothmund-Thomson syndrome (disorder)|Siemens syndrome|Skin lines|Symmetrical dyschromatosis of extremities|Symmetrical dyschromatosis of extremities (disorder)|Symmetrical progressive erythrokeratoderma|Systematised elastorrhexis|Systematized elastorrhexis|Systemic elastorrhexis|Thost-Unna diffuse palmoplantar keratoderma|Thost-Unna keratoderma|Trichodental syndrome|Trichodental syndrome (disorder)|Tylosis|Type 1 aplasia cutis|Type 3 aplasia cutis|Van Lohuizen's syndrome|Vascular neurocutaneous syndrome|Vascular neurocutaneous syndrome (disorder)|Vohwinkel's mutilating keratoderma|WSS - Wrinkly skin syndrome|Weary-Kindler syndrome|Winter erythrokeratolysis|Witkop-Von Sallmann disease|Witkop-von Sallman syndrome|Wrinkly skin syndrome|Wrinkly skin syndrome (disorder)|X-linked dyskeratosis congenita|X-linked dyskeratosis congenita (disorder)|Zinsser-Cole-Engman syndrome|Zinsser-Cole-Engmann syndrome|Zosteriform lentiginosis|Zosteriform lentiginosis (disorder)|Zosteriform porokeratosis

    ICD 10 CM 2017, (Clinical Modification) for coding of death certificates and mortality data. The international Statistical Classification of Diseases and Related Health Problems (ICD) 10th Revision and Clinical Modification. International Classification of Diseases, Tenth Revision, Clinical Modification.Q82.8 Other specified congenital malformations of skin and Thost-Unna diffuse palmoplantar keratoderma

    Thost-Unna diffuse palmoplantar keratoderma
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