Q82.8
BillableOther specified congenital malformations of skin
Other specified congenital malformations of skin
Status
Billable / Specific
Parent Code
Q82Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- 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]
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Congenital deficiency of pigment of skin1953005
- Congenital preauricular pit1955003
- Preauricular dimple1955003
- Preauricular pit1955003
- Achondrogenesis2391001
- Club nail4373005
- Clubbing of nail4373005
- Hippocratic nail4373005
- Hippocratic nails4373005
- Increased curvature of nails4373005
- BS - Bloom syndrome4434006
- Bloom syndrome4434006
- Congenital telangiectatic erythema syndrome4434006
- Keratosis spinulosa4859009
- Lichen spinulosus4859009
- KP - Keratosis pilaris5132005
- Keratosis pilaris5132005
- Congenital keratoderma6874009
- Dermatitis of the newborn7392002
- Inflammatory dermatosis of newborn7392002
- Neonatal dermatitis7392002
- Macroencephaly9740002
- Megalencephaly9740002
- Insulin receptor defect10680005
- Variation in hair color12168009
- Variation in hair colour12168009
- Multiple malformation syndrome with senile-like appearance12674005
- Clinodactyly17268007
- Congenital clinodactyly17268007
- Ambiguous genitalia21321009
- Keratoderma hereditarium mutilans24559001
- Mutilating keratoderma24559001
- Mutilating keratoderma of Vohwinkel24559001
- Vohwinkel syndrome24559001
- Vohwinkel's mutilating keratoderma24559001
- Acrocyanosis25003006
- Crocq's disease25003006
- Autosomal recessive hypohidrotic ectodermal dysplasia syndrome27025001
- Hypohidrotic autosomal recessive ectodermal dysplasia27025001
- Acroosteolysis27201004
- Congenital abnormality of sclera32809005
- Congenital anomaly of sclera32809005
- Clawfoot36755004
- Contracted foot36755004
- Pes cavus36755004
- Talipes cavus36755004
- Talipes plantaris36755004
- Juvenile periodontosis with hyperkeratosis40158001
- Papillon-Lefevre syndrome40158001
- Papillon-Lefèvre syndrome40158001
- Blue sacral spot40467008
- Mongolian blue spot40467008
- Mongolian macula40467008
- Mongolian spot40467008
- Multiple malformation syndrome, small stature, without skeletal dysplasia41483000
- Extramedullary haematopoiesis42952007
- Extramedullary hematopoiesis42952007
- Hypohidrosis45004005
- Hypohydrosis45004005
- Oligohidrosis45004005
- Congenital leuconychia47139007
- Congenital leukonychia47139007
- Darier disease48611009
- Darier's disease48611009
- Darier-White disease48611009
- Dyskeratosis follicularis48611009
- Keratosis follicularis48611009
- Psorospermosis48611009
- Psorospermosis follicularis vegetans48611009
- Cutis verticis gyrata51603000
- Clouston syndrome54209007
- Hidrotic ectodermal dysplasia54209007
- Hidrotic ectodermal dysplasia syndrome54209007
- Congenital hypotrichia56558005
- Congenital hypotrichosis56558005
- Hypotrichosis congenita56558005
- Chalazodermia58588007
- Cutis laxa58588007
- Dermatolysis58588007
- Dermatomegaly58588007
- Generalised elastolysis58588007
- Generalised elastorrhexis58588007
- Generalized elastolysis58588007
- Generalized elastorrhexis58588007
- Primary elastolysis58588007
- Systematised elastorrhexis58588007
- Systematized elastorrhexis58588007
- Systemic elastorrhexis58588007
- Diffuse dermatitis58921009
- Cutis laxa, autosomal recessive59451000
- Hair discoloration59571007
- Hair discolouration59571007
- Haemolytic anaemia with emphysema AND cutis laxa60805002
- Hemolytic anemia with emphysema AND cutis laxa60805002
- Congenital oculocutaneous hypopigmentation61649007
- Congenital clubbed nail64596006
- Congenital clubbing64596006
- Congenital clubnail64596006
- Poikiloderma congenitale69093006
- Poikiloderma congenitale syndrome69093006
- Rothmund-Thomson syndrome69093006
- Congenital poikiloderma70041004
- Erythrokeratodermia variabilis70041004
- Mendes da Costa syndrome70041004
- Congenital dermal sinus70499005
- Congenital cutaneous angiomatosis73716000
- Cutis laxa with bone dystrophy73856006
- Cutis laxa with joint laxity AND retarded development73856006
- Cutis laxa with osteodystrophy73856006
- Congenital scar74223008
- Cole-Engmann-Zinsser syndrome74911008
- Congenital dyskeratosis74911008
- DKC - Dyskeratosis congenita74911008
- Dyskeratosis congenita74911008
- Zinsser-Cole-Engman syndrome74911008
- Zinsser-Cole-Engmann syndrome74911008
- Benign familial chronic pemphigus79468000
- Familial benign chronic pemphigus79468000
- Familial benign pemphigus79468000
- Hailey Hailey disease79468000
- Hailey-Hailey disease79468000
- Mibelli's disease80432009
- Porokeratosis of Mibelli80432009
- Osteopathia striata82663009
- Voorhoeve's disease82663009
- Abnormal dermatoglyphic pattern83145004
- Dermatoglyphic abnormality83145004
- Dermatoglyphic anomalies83145004
- Accessory skin tags84449007
- Congenital accessory skin tag84449007
- Congenital melanosis86042009
- Achondroplasia86268005
- Achondroplastic dwarf86268005
- Achondroplastic dwarfism86268005
- Chondrodystrophia fetalis86268005
- Congenital osteosclerosis86268005
- Osteosclerosis congenita86268005
- Frontonasal dysplasia sequence86610004
- Median cleft face syndrome86610004
- Dominant autosomal hereditary disorder, incomplete penetrance87006007
- Classic EPF (eosinophilic pustular folliculitis)95333004
- Classic eosinophilic pustular folliculitis95333004
- Eosinophilic folliculitis95333004
- Eosinophilic pustular folliculitis95333004
- Ofuji disease95333004
- Ofuji's disease95333004
- Peripheral cyanosis95442007
- Abnormal plantar creases95469008
- Amelocerebrohypohidrotic syndrome109478007
- Epilepsy, dementia and amelogenesis imperfecta109478007
- Epilepsy, mental deterioration and yellow teeth109478007
- Kohlschutter syndrome109478007
- Kohlschutter's syndrome109478007
- Kohlschütter Tönz syndrome109478007
- Congenital retrognathism109515000
- Retrognathia109515000
- Retrognathism109515000
- Alveolar bone loss109706009
- Acrokerato-elastoidosis111029001
- Acrokeratoelastoidosis of Costa111029001
- PPKP3 - palmoplantar keratoderma punctate type 3111029001
- Punctate palmoplantar hyperkeratosis type 3111029001
- Punctate palmoplantar keratoderma type 3111029001
- Bennion Patterson syndrome111030006
- Howel Evans syndrome111030006
- Howel-Evans' syndrome111030006
- Howel-Evans-Clark syndrome111030006
- Keratoderma with carcinoma of esophagus111030006
- Keratoderma with carcinoma of oesophagus111030006
- Keratosis palmoplantaris esophageal carcinoma syndrome111030006
- Keratosis palmoplantaris oesophageal carcinoma syndrome111030006
- Palmoplantar hyperkeratosis esophageal carcinoma syndrome111030006
- Palmoplantar hyperkeratosis oesophageal carcinoma syndrome111030006
- Palmoplantar keratoderma esophageal carcinoma syndrome111030006
- Palmoplantar keratoderma oesophageal carcinoma syndrome111030006
- Tylosis esophageal carcinoma syndrome111030006
- Tylosis oesophageal carcinoma syndrome111030006
- LEOPARD syndrome111306001
- Leopard syndrome lentiginosis111306001
- Multiple lentigines syndrome111306001
- Cutis laxa, autosomal dominant111388003
- Dermatoglyphs165185004
- Dermatoglyphs - skin lines165185004
- Skin lines165185004
- Cafe au lait spots201281002
- Cafe-au-lait spots201281002
- Café au lait spot201281002
- Café au lait spots201281002
- Abnormal blue sclerae204164000
- Blue sclera204164000
- Central cleft lip204608004
- Abnormal palmar creases205557000
- Angiomatosis205562004
- Congenital pigmentary anomaly of skin205564003
- Congenital pigmentary skin anomalies205564003
- Brugsch syndrome205570009
- Brugsch's syndrome205570009
- FDH - Focal dermal hypoplasia205573006
- FODH - Focal dermal hypoplasia205573006
- Focal dermal hypoplasia205573006
- Goltz syndrome205573006
- Goltz-Gorlin syndrome205573006
- Hereditary benign acanthosis nigricans205583005
- Vascular neurocutaneous syndrome234139002
- Hyperpigmentation of oral mucosa235038002
- Melanin pigmentation of oral mucosa235038002
- Hereditary benign acanthosis nigricans with insulin resistance237606005
- Insulin receptor defect with insulin-resistant diabetes mellitus and acanthosis nigricans237606005
- Insulin-resistant acanthosis nigricans type A237606005
- Keratosis follicularis spinulosa decalvans238626006
- Keratosis pilaris decalvans238626006
- Linear porokeratosis238631008
- Zosteriform porokeratosis238631008
- Giant porokeratosis238632001
- Disseminated superficial porokeratosis238633006
- Benign acanthosis nigricans238634000
- Pseudoacanthosis nigricans238634000
- Livedo racemosa238772004
- Livedo reticularis238772004
- Anetoderma238828009
- Atrophoderma maculatum238828009
- Hereditary sclerosing poikiloderma238834002
- Weary-Kindler syndrome238834002
- Congenital bullous poikiloderma238836000
- Kindler epidermolysis bullosa238836000
- Kindler syndrome238836000
- Kindler's syndrome238836000
- Poikiloderma of Kindler238836000
- Extensive congenital erosions, vesicles and reticulate scarring238851009
- WSS - Wrinkly skin syndrome238875009
- Wrinkly skin syndrome238875009
- Fat hypertrophy238893005
- Genodermatosis239001006
- Dwarfism, alopecia, pseudoanodontia, cutis laxa239025003
- ANOTHER (alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy, respiratory tract infection) syndrome239050000
- ANOTHER syndrome239050000
- Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections239050000
- Hypohidrotic ectodermal dysplasia, hypothyroidism, ciliary dyskinesia syndrome239050000
- Multiple benign annular creases of extremities239053003
- Dowling-Degos syndrome239054009
- Reticulate pigmented anomaly of flexures239054009
- Acropachy239055005
- Hereditary acropachy239055005
- Hereditary clubbing239055005
- Hippocratic fingers239055005
- Flynn-Aird syndrome239056006
- Erythrokeratoderma progressiva of Gottron239063006
- Symmetrical progressive erythrokeratoderma239063006
- Erythrokeratolysis hiemalis239064000
- Keratolytic winter erythema239064000
- Oudtshoorn disease239064000
- Winter erythrokeratolysis239064000
- Familial continual skin peeling239065004
- Idiopathic deciduous skin239065004
- Keratolysis exfoliativa239065004
- Hereditary palmoplantar keratoderma239066003
- Palmoplantar keratoderma transgrediens239067007
- Acroerythrokeratoderma239069005
- Mal de Meleda239069005
- Meleda disease239069005
- Progressive palmoplantar keratoderma239070006
- Progressive palmoplantar keratoderma of Greither239070006
- Epidermolytic palmoplantar hyperkeratosis239071005
- Epidermolytic palmoplantar keratoderma of Vorner239071005
- Congenital palmoplantar and perioral keratoderma of Olmsted239072003
- Mutilating palmoplantar hyperkeratosis with periorificial keratotic plaques239072003
- Olmsted syndrome239072003
- Circumscribed palmoplantar keratoderma239073008
- Localised palmoplantar keratoderma239073008
- Localized palmoplantar keratoderma239073008
- Huriez syndrome239076000
- Keratoderma with scleroatrophy of extremities239076000
- Palmoplantar hyperkeratosis sclerodactyly syndrome239076000
- Palmoplantar keratoderma sclerodactyly syndrome239076000
- Scleroatrophic syndrome239076000
- Papuloverrucous palmoplantar keratoderma of Jakac-Wolf239078004
- Polykeratosis of Touraine239078004
- Inherited cutaneous hyperpigmentation239079007
- Dyschromatosis universalis239082002
- Melanism239082002
- Franceschetti-Jadassohn syndrome239084001
- Naegeli's syndrome239084001
- Naegeli-Franceschetti-Jadassohn syndrome239084001
- Acropigmentation of Dohi239085000
- Reticulate acropigmentation of Dohi239085000
- Symmetrical dyschromatosis of extremities239085000
- DPR - Dermatopathia pigmentosa reticularis239088003
- Dermatopathia pigmentosa reticularis239088003
- Hairy malformation of palms and soles239126004
- Elastic naevus239140003
- Elastic nevus239140003
- Naevus elasticus239140003
- Nevus elasticus239140003
- Lipomatous hypertrophy239142006
- Michelin-tire baby239142006
- Michelin-tyre baby239142006
- Congenital absence of skin on scalp239152005
- Nonsyndromic aplasia cutis congenita239152005
- Type 1 aplasia cutis239152005
- Congenital absence of skin on scalp with epidermal naevi239153000
- Congenital absence of skin on scalp with epidermal nevi239153000
- Type 3 aplasia cutis239153000
- Skin punctum247445007
- Palmar pit247449001
- Canities247564004
- White forelock247564004
- Simian crease248409006
- Single transverse palmar crease248409006
- PXE - Pseudoxanthoma elasticum252246005
- Pseudoxanthoma elasticum252246005
- Arrhythmogenic right ventricular cardiomyopathy253528005
- Arrhythmogenic right ventricular dysplasia253528005
- Hereditary acroosteolysis254148004
- Congenital ectodermal defect254154003
- Inherited disorder of keratinisation254214009
- Inherited disorder of keratinization254214009
- Erythrokeratoderma254215005
- Hereditary erythrokeratolysis254216006
- Hereditary acantholytic dermatosis254217002
- Hereditary follicular keratoses254218007
- Inherited cutis laxa254220005
- Neonatal cutis laxa with marfanoid phenotype254221009
- Cutis laxa, recessive, type I254222002
- Cutis laxa, recessive, type II254223007
- Hypotrichosis with keratosis pilaris and lentiginosis254227008
- Congenital woolly hair254231002
- Congenital wooly hair254231002
- Milia254679001
- Malignant melanoma arising in congenital naevus254734009
- Malignant melanoma arising in congenital nevus254734009
- CMTC - Cutis marmorata telangiectatica congenita254778000
- Congenital livedo reticularis254778000
- Cutis marmorata telangiectasia congenita254778000
- Cutis marmorata telangiectatica congenita254778000
- Van Lohuizen's syndrome254778000
- Blue naevus of skin254806009
- Blue nevus of skin254806009
- Trichodental syndrome277810000
- Juvenile elastoma277812008
- Recession of bone298358008
- Finding of palmar crease301323003
- Observation of palmar crease301323003
- Lump of palm307215008
- Mass of palm307215008
- Dysplasia of larynx308132000
- Diffuse palmoplantar keratoderma of Thost-Unna399955009
- Thost-Unna diffuse palmoplantar keratoderma399955009
- Thost-Unna keratoderma399955009
- Tylosis399955009
- Hereditary benign intraepithelial dyskeratosis400014002
- Witkop-Von Sallmann disease400014002
- Witkop-von Sallman syndrome400014002
- Acrokeratosis verruciformis of Darier disease400018004
- Keratosis rubra pilaris400043005
- Keratosis pilaris atrophicans400059005
- Porokeratosis400080004
- AKV - Acrokeratosis verruciformis400085009
- Acrokeratosis verruciformis of Hopf400085009
- Connective tissue hamartoma of skin400091006
- Connective tissue naevus400091006
- Connective tissue naevus of skin400091006
- Connective tissue nevus400091006
- Connective tissue nevus of skin400091006
- Dermal connective tissue hamartoma400091006
- Glycosaminoglycans naevus400091006
- Glycosaminoglycans nevus400091006
- Focal acral hyperkeratosis400115004
- Diffuse palmoplantar keratoderma400123002
- Hereditary diffuse palmoplantar keratoderma400123002
- Acanthosis nigricans402599005
- Autosomal dominant ichthyosis402770002
- Punctate palmoplantar keratoderma402773000
- Genetic syndrome with hypermelanosis402780003
- Inherited pseudoxanthoma elasticum402782006
- Zosteriform lentiginosis403539002
- Aplasia cutis congenita secondary to malformation syndrome (Type 9)403553002
- Delleman-Oorthuys syndrome403554008
- Oculocerebrocutaneous syndrome403554008
- Cutaneous lesion resulting from spina bifida403561007
- Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma403766000
- Rosenthal-Klöpfer syndrome403766000
- Hereditary sclerosing poikiloderma of Weary403774004
- Flexural Darier disease403783009
- Flexural Darier's disease403783009
- Hypertrophic Darier disease403784003
- Hypertrophic Darier's disease403784003
- Linear/nevoid/zosteriform Darier disease403785002
- Linear/nevoid/zosteriform Darier's disease403785002
- Acral Darier disease403786001
- Acral Darier's disease403786001
- Palmar pitting due to Darier disease403787005
- Palmar pitting due to Darier's disease403787005
- Nail dystrophy due to Darier disease403788000
- Nail dystrophy due to Darier's disease403788000
- Nail dystrophy due to Hailey-Hailey disease403789008
- Nail dystrophy due to benign familial pemphigus403789008
- Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu403790004
- Autosomal recessive familial woolly hair403795009
- Autosomal recessive familial wooly hair403795009
- Autosomal dominant pseudoxanthoma elasticum403811007
- Autosomal recessive pseudoxanthoma elasticum403812000
- Gronblad Strandberg Touraine syndrome403812000
- Gronblad Strandberg syndrome403812000
- Localised congenital cutis laxa403813005
- Localized congenital cutis laxa403813005
- Cutis laxa secondary to inherited disorder of connective tissue403814004
- Neonatal eosinophilic pustular folliculitis403845000
- Neonatal ofuji's disease403845000
- Hyperplasia of gingiva441798003
- Hyperplastic gingiva441798003
- M-CM - macrocephaly capillary malformation700063005
- MCAP - megalencephaly capillary malformation700063005
- Macrocephaly-capillary malformation700063005
- Macrocephaly-cutis marmorata telangiectatica congenita700063005
- Megalencephaly capillary malformation700063005
- Megalencephaly, capillary malformation, polymicrogyria syndrome700063005
- Beare-Stevenson cutis gyrata syndrome703528008
- Cutis gyrata syndrome of Beare and Stevenson703528008
- Cutis gyrata, acanthosis nigricans, craniosynostosis syndrome703528008
- Corneal leucoma704272003
- Corneal leukoma704272003
- Palmoplantar keratoderma706885006
- Keratoderma707209001
- Autosomal recessive dyskeratosis congenita707272006
- Autosomal dominant dyskeratosis congenita707273001
- Hoyeraal-Hreidarsson syndrome707276009
- Chronic haemolytic anaemia707480001
- Chronic hemolytic anemia707480001
- X-linked dyskeratosis congenita708536001
- Acral peeling skin syndrome709416009
- Peeling skin syndrome, acral type709416009
- Cole disease711154007
- Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification711154007
- Keratoderma with woolly hair type I715535009
- Keratoderma with wooly hair type I715535009
- Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome715535009
- Naxos disease715535009
- Palmoplantar hyperkeratosis with arrhythmogenic cardiomyopathy715535009
- Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type716105001
- Non-epidermolytic palmoplantar keratoderma716105001
- Camisa disease717183001
- Keratoderma hereditarium mutilans with ichthyosis syndrome717183001
- Keratoderma ichthyosiform dermatosis elevated beta-glucuronidase syndrome717183001
- Vohwinkel ichthyosis syndrome717183001
- Buschke Fischer Brauer syndrome717184007
- Keratodermia palmoplantaris papulosa Buschke Fischer Brauer type717184007
- Punctate palmoplantar keratoderma type 1717184007
- Porokeratosis plantaris palmaris et disseminata718218005
- Autosomal recessive palmoplantar keratoderma and congenital alopecia Wallis type719104003
- Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome719104003
- Autosomal dominant palmoplantar keratoderma and congenital alopecia719518004
- Palmoplantar keratoderma and congenital alopecia Stevanovic type719518004
- Absence of dermatoglyphics with congenital milia syndrome719595002
- Absence of fingerprints with congenital milia syndrome719595002
- Baird syndrome719595002
- Carvajal syndrome719835006
- Keratoderma with woolly hair type II719835006
- Keratoderma with wooly hair type II719835006
- Woolly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome719835006
- Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome719835006
- CDAGS (craniosynostosis, clavicular hypoplasia, delayed closure of fontanelle, anal anomalies, genitourinary malformations, skin eruption) syndrome720812002
- CDAGS syndrome720812002
- Craniosynostosis, anal anomaly, porokeratosis syndrome720812002
- Deaf blind hypopigmentation syndrome Yemenite type721084001
- Warburg Thomsen syndrome721084001
- Diffuse palmoplantar keratoderma and acrocyanosis syndrome721096008
- Ectodermal dysplasia with skin anomaly and intellectual disability721147000
- Halal Setton Wang syndrome721147000
- Hidrotic ectodermal dysplasia Halal type721147000
- MIDAS syndrome721879006
- MIDAS syndrome (microphthalmia, dermal aplasia, sclerocornea) syndrome721879006
- Microphthalmia with linear skin defect syndrome721879006
- Syndromic microphthalmia type 7721879006
- Erythrokeratodermia variabilis 3722035007
- Erythrokeratodermia variabilis Kamouraska type722035007
- Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome722035007
- MEDNIK (mental retardation, enteropathy, deafness, peripheral neuropathy, ichtyosis, keratodermia) syndrome722035007
- MEDNIK syndrome722035007
- Hernandez Fragoso syndrome722113001
- Osteoporosis and oculocutaneous hypopigmentation syndrome722113001
- Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome722201004
- Pai syndrome722201004
- Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome722202006
- Palmoplantar keratoderma with deafness syndrome722203001
- Palmoplantar keratoderma Nagashima type722205008
- Fitzsimmons McLachlan Gilbert syndrome722209002
- Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome722209002
- CEDNIK (cerebral dysgenesis, neuropathy, ichthyosis, keratoderma) syndrome722385008
- CEDNIK syndrome722385008
- Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome722385008
- Congenital lethal erythroderma722391005
- Congenital atrophy of optic nerve722990003
- Congenital optic atrophy722990003
- MACS (macrocephaly, alopecia, cutis laxa, scoliosis) syndrome723367005
- MACS syndrome723367005
- Macrocephaly, alopecia, cutis laxa, scoliosis syndrome723367005
- RIN2 deficiency723367005
- Tall forehead, sparse hair, skin hyperextensibility, scoliosis syndrome723367005
- Trichothiodystrophy723551003
- Terminal osseous dysplasia and pigmentary defect syndrome723578001
- Keratosis follicularis, dwarfism, cerebral atrophy syndrome723830005
- Elejalde disease724091002
- Neuroectodermal melanolysosomal disease724091002
- Keratosis palmaris et plantaris with clinodactyly syndrome724224007
- Palmoplantar keratoderma with clinodactyly syndrome724224007
- Familial continuous skin peeling syndrome724838009
- Hereditary skin peeling syndrome724838009
- Peeling skin syndrome724838009
- Melanosis of mucosa of body orifice724847001
- Mucosal melanosis724847001
- CAMOS (cerebellar ataxia, mental retardation, optic atrophy, skin abnormalities) syndrome726031001
- CAMOS syndrome726031001
- Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome726031001
- SCAR5 - spinocerebellar ataxia autosomal recessive 5726031001
- Dermatoleukodystrophy733044009
- Exostosis, anetoderma, brachydactyly type E syndrome733416004
- Exostosis, anetodermia, brachydactyly type E syndrome733416004
- Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome733469003
- Hypo-and hypermelanotic cutaneous macules, retarded growth, intellectual disability syndrome733469003
- Westerhof Beemer Cormane syndrome733469003
- SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome734173003
- SCARF syndrome734173003
- Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome734173003
- Dysmorphism, cleft palate, loose skin syndrome763278004
- Facial dysmorphism, cleft palate, loose skin syndrome763278004
- Cantu craniofaciofrontodigital syndrome763320005
- Craniofaciofrontodigital syndrome763320005
- Familial progressive hyper and hypopigmentation763368004
- Familial progressive hyperpigmentation and hypopigmentation of skin763368004
- Antinolo Nieto Borrego syndrome763402002
- Spastic paraplegia, neuropathy, poikiloderma syndrome763402002
- HOPP syndrome763658004
- Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome763658004
- CHACS - curly hair, acral keratoderma, caries syndrome763686007
- Curly hair, acral keratoderma, caries syndrome763686007
- Congenital absence of fingerprints763748007
- Immigration delay disease763748007
- Isolated congenital adermatoglyphia763748007
- KLICK syndrome763775000
- Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome763775000
- Leukonychia totalis763792009
- Keratoderma with woolly hair type IV764108000
- Keratoderma with wooly hair type IV764108000
- Woolly hair with palmoplantar keratoderma syndrome764108000
- Wooly hair with palmoplantar keratoderma syndrome764108000
- Keratosis palmoplantaris striata764958008
- Keratosis palmoplantaris striata et areata764958008
- Keratosis palmoplantaris varians of Wachters764958008
- Striate palmoplantar keratoderma764958008
- Focal palmoplantar and gingival keratoderma764963007
- Ectodermal dysplasia short stature syndrome764995008
- Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome764995008
- Short stature, nail dysplasia, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome764995008
- Primary essential cutis verticis gyrata765135003
- Familial generalised lentiginosis765195000
- Familial generalized lentiginosis765195000
- Familial lentigines profusa765195000
- Familial multiple lentigines syndrome without systemic involvement765195000
- Sparse hair, short stature, skin anomalies syndrome771182002
- Thumb deformity, alopecia, pigmentation anomaly syndrome771182002
- PARC (poikiloderma, alopecia, retrognathism, cleft palate) syndrome771186004
- PARC syndrome771186004
- Poikiloderma, alopecia, retrognathism, cleft palate syndrome771186004
- Christianson Fourie syndrome771239007
- Hidrotic ectodermal dysplasia Christianson Fourie type771239007
- Torticollis, keloids, cryptorchidism, renal dysplasia syndrome771266007
- PENS (papular epidermal naevi with skyline basal cell layers) syndrome771473004
- PENS (papular epidermal nevi with skyline basal cell layers) syndrome771473004
- PENS syndrome771473004
- Papular epidermal naevi with skyline basal cell layers syndrome771473004
- Papular epidermal nevi with skyline basal cell layers syndrome771473004
- Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome773553003
- Shaheen syndrome773553003
- Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome773577009
- CEVD - congenital erosive and vesicular dermatosis773691007
- Congenital erosive and vesicular dermatosis773691007
- Congenital erosive and vesicular dermatosis with reticulated supple scarring773691007
- Leukonychia totalis, acanthosis-nigricans-like lesions, abnormal hair syndrome773700005
- Congenital erythroderma, hypotrichosis, recurrent infections, multiple food allergies syndrome774211005
- SAM syndrome774211005
- Severe dermatitis, multiple allergies, metabolic wasting syndrome774211005
- Skin fragility, wooly hair, palmoplantar keratoderma syndrome778010006
- Skin fragillity, woolly hair, palmoplantar keratoderma syndrome778010006
- Primary non-essential cutis verticis gyrata778044004
- Focal palmoplantar keratoderma with joint keratoses778051008
- Diffuse palmoplantar keratoderma with painful fissures778062008
- ARCL2B - autosomal recessive cutis laxa type 2B778068007
- Autosomal recessive cutis laxa type 2 progeroid type778068007
- Autosomal recessive cutis laxa type 2B778068007
- Hereditary sensorimotor neuropathy with hyperelastic skin782881002
- Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering783136007
- OPD (otopalatodigital) spectrum disorder784010006
- Otopalatodigital syndrome spectrum disorder784010006
- ARCL1C - autosomal recessive cutis laxa type 1C784349004
- Autosomal recessive cutis laxa type 1C784349004
- Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies784349004
- Urban Rifkin Davis syndrome784349004
- ARCL2A - autosomal recessive cutis laxa type 2A784381008
- Autosomal recessive cutis laxa type 2A784381008
- Palmoplantar keratoderma, spastic paralysis syndrome785725008
- Powell Venencie Gordon syndrome785725008
- Osteopathia striata, pigmentary dermopathy, white forelock syndrome787408008
- Whyte Murphy syndrome787408008
- SADDAN (severe achondroplasia, developmental delay, acanthosis nigricans) syndrome874931001
- Severe achondroplasia, developmental delay, acanthosis nigricans syndrome874931001
- Microphthalmos due to Delleman syndrome1003369001
- Congenital clinodactyly of finger1003620005
- Congenital crooked finger1003620005
- Congenital clinodactyly of fifth digit of hand1003621009
- Congenital clinodactyly of little finger1003621009
- Rothmund Thomson syndrome type 11003922004
- Rothmund Thomson syndrome type 21003923009
- Agenesis of distal interphalangeal flexion crease1010489008
- Congenital complete absence of distal interphalangeal skin crease1010489008
- Agenesis of interphalangeal skin crease1010490004
- Agenesis of phalangeal flexion crease1010490004
- Congenital absence of phalangeal crease1010490004
- Congenital complete absence of interphalangeal skin crease1010490004
- Agenesis of distal interphalangeal flexion crease of ring finger1010492007
- Congenital complete absence of distal interphalangeal skin crease of ring finger1010492007
- Agenesis of proximal interphalangeal flexion crease1010494008
- Agenesis of proximal interphalangeal skin crease1010494008
- Congenital complete absence of proximal interphalangeal skin crease1010494008
- Systematised linear porokeratosis1119290007
- Systematized linear porokeratosis1119290007
- Congenital extramedullary dermal haematopoiesis1142089004
- Congenital extramedullary dermal hematopoiesis1142089004
- Aplasia of palmar crease1144444005
- Aplasia of ring finger1144457002
- Congenital hypoplasia of pilosebaceous apparatus1144545009
- Congenital hypoplastic pilosebaceous unit1144545009
- Congenital hypoplasia of skin1144858003
- Congenital hypoplasia of apocrine gland of axilla1144877001
- Congenital hypoplasia of eccrine gland1144879003
- Congenital hypoplasia of sudoriferous gland1144879003
- Congenital hypoplasia of sweat gland1144880000
- Congenital hypoplasia of sebaceous gland1144881001
- Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome1172629005
- EKC (erythrokeratodermia cardiomyopathy) syndrome1179293006
- Erythrokeratodermia cardiomyopathy syndrome1179293006
- Congenital corneal leucoma1217688006
- Congenital corneal leukoma1217688006
- KRT1-related diffuse NEPPK (nonepidermolytic palmoplantar keratoderma)1222645005
- KRT1-related diffuse nonepidermolytic keratoderma1222645005
- Keratin 1-related diffuse nonepidermolytic palmoplantar keratoderma1222645005
- Palmoplantar keratoderma, Charcot-Marie-Tooth syndrome1222646006
- Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome1222646006
- Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome1230005002
- Isolated focal non-epidermolytic palmoplantar keratoderma1260463008
- Mosaic Legius syndrome1300197001
- Mosaic NF1 (neurofibromatosis 1) like syndrome1300197001
- Mosaic neurofibromatosis 1-like syndrome1300197001
- Congenital skin contracture10624871000119109
- Lipoma of brain15863451000119107
UMLS
- DermatomegalyC0010495
- ElastolysisC0010495
- ChalazodermaC0010495
- ChalazodermiaC0010495
- Cutaneous laxityC0010495
- Cutis LaxaC0010495
- Cutis laxaC0010495
- Cutis laxa (disorder)C0010495
- Cutis laxa (hyperelastica)C0010495
- DermatochalasiaC0010495
- DermatolysesC0010495
- DermatolysisC0010495
- Hypoelastic skinC0010495
- Inelastic skinC0010495
- Lax skinC0010495
- Loose and inelastic skinC0010495
- Loose skinC0010495
- Primary elastolysisC0010495
- Skin laxityC0010495
- chalastodermiaC0010495
- chalazodermiaC0010495
- cutis laxaC0010495
- dermatochalasiaC0010495
- dermatochalasisC0010495
- dermatochalaziaC0010495
- dermatolysisC0010495
- dermatomegalyC0010495
- elastolysisC0010495
- lax skinC0010495
- loose skinC0010495
- looses skinC0010495
- skin laxityC0010495
- Abnormal dermatoglyphic patternC0432333
- Abnormal dermatoglyphic pattern (disorder)C0432333
- Abnormal dermatoglyphicsC0432333
- Abnormal fingerprintsC0432333
- Dermatoglyphic abnormalitiesC0432333
- Dermatoglyphic abnormalityC0432333
- Dermatoglyphic anomaliesC0432333
- Dermatoglyphic anomalyC0432333
- Dermatoglyphic anomaly NOSC0432333
- Abnormal palmar creaseC0221199
- Abnormal palmar creasesC0221199
- Abnormal palmar creases (disorder)C0221199
- Abnormality of the palm linesC0221199
- Abnormality of the palmar creasesC0221199
- Accessory skin tagsC0265988
- Congenital accessory skin tagC0265988
- Congenital accessory skin tag (disorder)C0265988
- BCPMC0085106
- BENIGN CHRONIC PEMPHIGUSC0085106
- Benign Chronic PemphigusC0085106
- Benign Familial PemphigusC0085106
- Benign chronic pemphigusC0085106
- Benign familial chronic pemphigusC0085106
- Benign familial pemphigusC0085106
- Benign familial pemphigus [Hailey-Hailey]C0085106
- Chronic Benign Familial PemphigusC0085106
- Familial Benign Chronic PemphigusC0085106
- Familial Benign PemphigusC0085106
- Familial Pemphigus, BenignC0085106
- Familial benign chronic pemphigusC0085106
- Familial benign pemphigusC0085106
- Familial benign pemphigus (disorder)C0085106
- HAILEY HAILEY DISC0085106
- HAILEY-HAILEY DISEASEC0085106
- HHDC0085106
- Hailey Hailey DiseaseC0085106
- Hailey Hailey diseaseC0085106
- Hailey-Hailey DiseaseC0085106
- Hailey-Hailey diseaseC0085106
- PEMPHIGUS, BENIGN FAMILIALC0085106
- Pemphigus, Benign FamilialC0085106
- Pemphigus, benign familialC0085106
- benign familial pemphigusC0085106
- diseases hailey haileyC0085106
- hailey diseaseC0085106
- hailey hailey diseaseC0085106
- hailey-hailey diseaseC0085106
- Congenital PoikilodermaC0032339
- Congenital poikilodermaC0032339
- Congenitale, PoikilodermaC0032339
- Congenitales, PoikilodermaC0032339
- POIKILODERMA ATROPHICANS AND CATARACTC0032339
- POIKILODERMA CONGENC0032339
- Poikiloderma Atrophicans and CataractC0032339
- Poikiloderma CongenitaleC0032339
- Poikiloderma Congenitale of Rothmund-ThomsonC0032339
- Poikiloderma CongenitalesC0032339
- Poikiloderma atrophicans and cataractC0032339
- Poikiloderma congenitaleC0032339
- Poikiloderma congenitale of Rothmund-ThomsonC0032339
- Poikiloderma congenitale syndromeC0032339
- Poikiloderma of Rothmund ThomsonC0032339
- Poikiloderma of Rothmund-ThomsonC0032339
- Poikiloderma, congenitalC0032339
- ROTHMUND-THOMSON SYNDROMEC0032339
- RTSC0032339
- Rothmund Thomson SyndromeC0032339
- Rothmund-Thomson PoikilodermaC0032339
- Rothmund-Thomson PoikilodermasC0032339
- Rothmund-Thomson SyndromeC0032339
- Rothmund-Thomson syndromeC0032339
- Rothmund-Thomson syndrome (disorder)C0032339
- Syndrome, Rothmund-ThomsonC0032339
- poikiloderma congenitaleC0032339
- rothmund thomson syndromeC0032339
- rothmund-thomson syndromeC0032339
- Inherited keratosis palmaris et plantarisC2910342
- Keratosis follicularis [Darier-White]C2910343
- Other specified congenital malformations of skinC2363246
Frequently Asked Questions
What is ICD-10 code Q82.8?
ICD-10-CM code Q82.8 represents "Other specified congenital malformations of skin". It is a billable/specific code that can be used on a claim.
Is Q82.8 a billable code?
Yes, Q82.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q82.8 in?
Q82.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q82.8?
Q82.8 has Excludes1 notes indicating codes that cannot be used together with it, including: acrodermatitis enteropathica (E83.2); congenital erythropoietic porphyria (E80.0); pilonidal cyst or sinus (L05.-); and 2 more.
What SNOMED CT codes does Q82.8 map to?
Q82.8 maps to 299 SNOMED CT concepts: 400085009, 239050000, 784349004, 784381008, 778068007, and 294 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q82.8?
Q82.8 is linked to 9 UMLS Concept Unique Identifiers: C0010495, C0432333, C0221199, C0265988, C0085106, and 4 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.