Q82.4
BillableEctodermal dysplasia (anhidrotic)
Ectodermal dysplasia (anhidrotic)
Status
Billable / Specific
Parent Code
Q82Coding Notes
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
- Autosomal dominant KID (keratitis, ichthyosis, deafness) syndrome2625009
- Autosomal dominant keratitis, ichthyosis, deafness syndrome2625009
- Senter syndrome2625009
- Congenital anomaly of macula4041005
- Anhidrotic ectodermal dysplasia7731005
- Anhidrotic ectodermal dysplasia syndrome7731005
- Autosomal dominant hypohidrotic ectodermal dysplasia syndrome7731005
- Hypohidrotic ectodermal dysplasia syndrome7731005
- Rapp-Hodgkin ectodermal dysplasia syndrome7731005
- Rapp-Hodgkin type of ectodermal dysplasia7731005
- Ectodermal dysplasia8654005
- Congenital hypoplasia of breast8915006
- Hypoplasia of breast8915006
- Hypoplastic breast8915006
- Accelerated tooth eruption16000003
- Precocious dentition16000003
- Precocious tooth eruption16000003
- Premature tooth eruption16000003
- Schinzel-Giedion syndrome18899000
- ANN - Anonychia23610003
- Anonychia23610003
- Congenital absent nails23610003
- Nail dystrophy, deafness syndrome26718008
- Robinson nail dystrophy-deafness syndrome26718008
- Robinson's syndrome26718008
- Robinson-type ectodermal dysplasia26718008
- Ectodermal dysplasia-ocular malformation syndrome31291009
- Marshall syndrome33410002
- Marshall's syndrome33410002
- Amelogenesis imperfecta - osteosclerosis syndrome38993008
- TDO - Trichodento-osseous syndrome38993008
- TDO syndrome38993008
- Taurodontism - curly hair - osteosclerosis syndrome38993008
- Tricho-dento-osseous syndrome38993008
- Trichodento-osseous syndrome38993008
- Hypohidrosis45004005
- Hypohydrosis45004005
- Oligohidrosis45004005
- AEC - Ankyloblepharon, ectodermal defects, cleft lip and palate55821006
- AEC syndrome55821006
- Ankyloblepharon, ectodermal defects, cleft lip and palate55821006
- Ankyloblepharon-ectodermal dysplasia-clefting syndrome55821006
- Hay Wells syndrome of ectodermal dysplasia55821006
- Hay-Wells syndrome55821006
- Hay-Wells syndrome of ectodermal dysplasia55821006
- Congenital hypotrichia56558005
- Congenital hypotrichosis56558005
- Hypotrichosis congenita56558005
- Neonatal tooth58748004
- Johanson-Blizzard syndrome75979009
- Dominant autosomal hereditary disorder, incomplete penetrance87006007
- Hyperpigmentation of oral mucosa235038002
- Melanin pigmentation of oral mucosa235038002
- Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes237610008
- Ectodermal dysplasia with hair-tooth-nail-sweating defect239006001
- Hypohidrotic ectodermal dysplasia239006001
- CST - Christ-Siemens-Touraine syndrome239007005
- Christ-Siemens-Touraine syndrome239007005
- Hypohidrotic X-linked ectodermal dysplasia239007005
- Roselli-Gulienetti ectodermal dysplasia239009008
- Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia239010003
- Basan syndrome239011004
- Greither type of ectodermal dysplasia239012006
- Anonychia with bizarre flexural pigmentation239013001
- TOD - Tricho-onychodental dysplasia239014007
- Tricho-onychodental dysplasia239014007
- Ectodermal dysplasia with hair-tooth-nail defects239015008
- Odonto-onychial dysplasia with alopecia239019002
- Fried tooth and nail syndrome239020008
- Fried's tooth and nail syndrome239020008
- Salamon syndrome239023005
- Salamon's syndrome239023005
- Ectodermal dysplasia, syndactyly and pili torti239024004
- Fleck syndrome239026002
- Hypohidrosis-diabetes insipidus syndrome239026002
- Ectodermal dysplasia with hair-tooth defects239027006
- Berlin syndrome239032007
- Ectodermal dysplasia with hair-nail defect239035009
- Tricho-oculodermovertebral syndrome239036005
- CHANDS - Curly hair, ankyloblepharon, nail dysplasia syndrome239037001
- Curly hair, ankyloblepharon, nail dysplasia syndrome239037001
- Kirman syndrome239038006
- Ectodermal dysplasia with tooth-nail defects239040001
- Ectodermal dysplasia with tooth-sweating defect239042009
- Sandman-Andra syndrome239043004
- Ectodermal dysplasia with nail defect239046007
- Ectodermal dysplasia with sweating defect239048008
- Cutaneous syndrome with ichthyosis239057002
- Ichthyosis hystrix Rheydt type239059004
- KID syndrome239059004
- KID/HID syndrome239059004
- KIDS - Keratitis ichthyosis and deafness syndrome239059004
- Keratitis ichthyosis and deafness syndrome239059004
- Keratitis ichthyosis deafness syndrome239059004
- Keratitis, ichthyosis, deafness/hystrix-like ichthyosis deafness syndrome239059004
- Cranioectodermal dysplasia254093009
- Sensenbrenner's syndrome254093009
- Acrofacial dysostosis Weyers type277807007
- Curry-Hall syndrome277807007
- Weyers acrodental dysostosis277807007
- Weyers acrofacial dysostosis277807007
- Ectodermal dysplasia with tooth-nail-sweating defect399974001
- Acanthosis nigricans402599005
- Ectodermal syndrome with hair-tooth-sweating defects402767001
- Ectodermal syndrome with hair-sweating defects402768006
- Autosomal dominant ichthyosis402770002
- Odonto-onycho-dermal dysplasia403762003
- Odontomicronychial ectodermal dysplasia403764002
- Anhidrotic ectodermal dysplasia with immune deficiency703525006
- Anhidrotic ectodermal dysplasia with immunodeficiency703525006
- Hypohidrotic ectodermal dysplasia with immune deficiency703525006
- Cerebellar ataxia and ectodermal dysplasia715371006
- Cerebellar ataxia co-occurrent with ectodermal dysplasia715371006
- Amelo-onycho-hypohidrotic syndrome715404000
- Ameloonychohypohidrotic syndrome715404000
- Ectodermal dysplasia with natal teeth Turnpenny type715576000
- Cleft lip and cleft palate with ectodermal dysplasia syndrome716248001
- Cleft lip and palate with syndactyly and pili torti716248001
- Zlotogora Ogur syndrome716248001
- Zlotogora Zilberman Tenenbaum syndrome716248001
- Blepharo-cheilo-odontic syndrome717911008
- Blepharocheilodontic syndrome717911008
- Clefting, ectropion, conical teeth syndrome717911008
- Elsching syndrome717911008
- BRESEK (brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia) syndrome717945001
- BRESEK syndrome717945001
- Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome717945001
- Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome717945001
- X-linked mental retardation Reish type717945001
- Ectodermal dysplasia with acanthosis nigricans syndrome719429003
- Lelis syndrome719429003
- Trichodysplasia with amelogenesis imperfecta syndrome719911000
- Contracture with ectodermal dysplasia and orofacial cleft syndrome720746006
- Ladda Zonana Ramer syndrome720746006
- EEM (ectodermal dysplasia, ectrodactyly, macular dystrophy) syndrome720856002
- EEM syndrome720856002
- Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome720856002
- Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome720986005
- Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema syndrome720986005
- OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema) syndrome720986005
- OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema) syndrome720986005
- Dermo odontodysplasia721091003
- Dermo-odonto dysplasia721091003
- Dermoodonto dysplasia721091003
- Ectodermal dysplasia with blindness syndrome721208007
- Limb mammary syndrome721972001
- Oculoosteocutaneous syndrome722061006
- Odonto-tricho-ungual-digito-palmar syndrome722063009
- Odonto-tricho-ungual-digito-palmar syndrome Mendoza-Valiente type722063009
- Odontotrichoungual-digital-palmar syndrome722063009
- Ackerman syndrome722280000
- Book syndrome722296002
- Trichothiodystrophy723551003
- Melanosis of mucosa of body orifice724847001
- Mucosal melanosis724847001
- Ectodermal dysplasia and sensorineural deafness syndrome732953008
- Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome734017008
- Ectodermal dysplasia trichoodontoonychial type734018003
- Pinheiro, Freire Maia, Miranda syndrome763620003
- Trichodermodysplasia and dental alterations syndrome763620003
- Odonto onycho dysplasia with alopecia syndrome763828007
- Odonto-onycho dysplasia alopecia syndrome763828007
- 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
- Trichoodontoonychial dysplasia766813000
- Trichoodontoonychial dysplasia with bone deficiency in frontoparietal region766813000
- Euhidrotic ectodermal dysplasia771240009
- Kopysc Barczyk Krol syndrome771240009
- Pilodental dysplasia, refractive errors syndrome771240009
- Ectodermal dysplasia syndactyly syndrome771335004
- Dermotrichic syndrome782916003
- Arthrogryposis and ectodermal dysplasia syndrome786039009
- Arthrogryposis, ectodermal dysplasia, other anomalies syndrome786039009
- Stoll Alembik Finck syndrome786039009
- FFDD - focal facial dermal dysplasia789156003
- Focal facial dermal dysplasia789156003
- Bitemporal aplasia cutis congenita789157007
- Brauer syndrome789157007
- FFDD type 1 - focal facial dermal dysplasia type 1789157007
- Focal facial dermal dysplasia 1 Brauer type789157007
- Focal facial dermal dysplasia type I789157007
- FFDD type 2 - focal facial dermal dysplasia type 2789159005
- Focal facial dermal dysplasia 2 Brauer Setleis type789159005
- Focal facial dermal dysplasia type II789159005
- FFDD type 3 - focal facial dermal dysplasia type 3789160000
- Focal facial dermal dysplasia 3 Setleis type789160000
- Focal facial dermal dysplasia type III789160000
- Setleis syndrome789160000
- FFDD type 4 - focal facial dermal dysplasia type 4789161001
- Focal facial dermal dysplasia type IV789161001
- Focal facial preauricular dysplasia789161001
- Onycho-tricho-dysplasia neutropenia syndrome1003381002
- Trichothiodystrophy type G1003381002
- Sabinas brittle hair syndrome1003920007
- Congenital hypoplasia of nail unit1144442009
- Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies1208985003
- RHOA (ras homolog family member A) related mosaic ectodermal dysplasia1208985003
- RHOA-related mosaic ectodermal dysplasia1208985003
- Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome1279835008
- Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA GOF (gain of function) mutation1354646005
- Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation1354646005
- Anhidrotic ectodermal dysplasia with immune deficiency due to NFKBIA gain of function mutation1354646005
- Anhidrotic ectodermal dysplasia with immune deficiency due to nuclear factor kappa-B inhibitor alpha, gain of function mutation1354646005
- Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB GOF mutation1366698006
- Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB gain of function mutation1366698006
UMLS
- Anhidrotic Ectodermal DysplasiaC1706004
- Anhidrotic Ectodermal DysplasiasC1706004
- Anhidrotic ectodermal dysplasiaC1706004
- Anhidrotic ectodermal dysplasia syndromeC1706004
- Anhidrotic, Ectodermal DysplasiaC1706004
- Anhidrotics, Ectodermal DysplasiaC1706004
- Anhydrotic Ectodermal DysplasiaC1706004
- Anhydrotic Ectodermal DysplasiasC1706004
- Dysplasia Anhidrotic, EctodermalC1706004
- Dysplasia Anhidrotics, EctodermalC1706004
- Dysplasia, Anhidrotic EctodermalC1706004
- Dysplasia, Anhydrotic EctodermalC1706004
- Dysplasias, Anhidrotic EctodermalC1706004
- Dysplasias, Anhydrotic EctodermalC1706004
- Ectodermal Dysplasia AnhidroticC1706004
- Ectodermal Dysplasia, AnhidroticC1706004
- Ectodermal Dysplasia, AnhydroticC1706004
- Ectodermal Dysplasias, AnhidroticC1706004
- Ectodermal Dysplasias, AnhydroticC1706004
- Ectodermal dysplasia (anhidrotic)C1706004
- Ectodermal dysplasia, anhidroticC1706004
Frequently Asked Questions
What is the ICD-10 code for ectodermal dysplasia (anhidrotic)?
The ICD-10-CM code for ectodermal dysplasia (anhidrotic) is Q82.4. The full clinical description is "Ectodermal dysplasia (anhidrotic)". Q82.4 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q82.4 mean?
ICD-10-CM code Q82.4 represents "Ectodermal dysplasia (anhidrotic)". It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q82.4 a billable code?
Yes, Q82.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q82.4 in?
Q82.4 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q82.4?
Q82.4 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 Q82.4 map to?
Q82.4 maps to 100 SNOMED CT concepts: 55821006, 23610003, 402599005, 16000003, 722280000, and 95 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q82.4?
Q82.4 is linked to 1 UMLS Concept Unique Identifier: C1706004. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.