Cutaneous syndrome with ichthyosis
Dysplasia Anhidrotic, Ectodermal
Fried tooth and nail syndrome
CHANDS - Curly hair, ankyloblepharon, nail dysplasia syndrome
AEC - Ankyloblepharon, ectodermal defects, cleft lip and palate
Cerebellar ataxia and ectodermal dysplasia
Dermo-odonto dysplasia
Oculoosteocutaneous syndrome
Salamon's syndrome
Senter syndrome
Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema syndrome
Focal facial dermal dysplasia 3 Setleis type
Greither type of ectodermal dysplasia
Hypohidrosis-diabetes insipidus syndrome
Dysplasia Anhidrotics, Ectodermal
Hay Wells syndrome of ectodermal dysplasia
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome
Precocious tooth eruption
Anhidrotic Ectodermal Dysplasia
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation
Hypohidrotic ectodermal dysplasia
Rapp-Hodgkin ectodermal dysplasia syndrome
Odonto-onycho dysplasia alopecia syndrome
Ankyloblepharon, ectodermal defects, cleft lip and palate
Anhidrotic ectodermal dysplasia with immune deficiency due to NFKBIA gain of function mutation
KIDS - Keratitis ichthyosis and deafness syndrome
Arthrogryposis, ectodermal dysplasia, other anomalies syndrome
Book syndrome
Focal facial dermal dysplasia 1 Brauer type
Autosomal dominant keratitis, ichthyosis, deafness syndrome
Dermoodonto dysplasia
Ectodermal dysplasia with blindness syndrome
Pinheiro, Freire Maia, Miranda syndrome
Ichthyosis hystrix Rheydt type
CST - Christ-Siemens-Touraine syndrome
Melanosis of mucosa of body orifice
Anhidrotic ectodermal dysplasia with immune deficiency due to nuclear factor kappa-B inhibitor alpha, gain of function mutation
Curly hair, ankyloblepharon, nail dysplasia syndrome
Tricho-oculodermovertebral syndrome
OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema) syndrome
TOD - Tricho-onychodental dysplasia
Christ-Siemens-Touraine syndrome
Cleft lip and palate with syndactyly and pili torti
Salamon syndrome
Robinson-type ectodermal dysplasia
Ectodermal Dysplasias, Anhydrotic
Congenital anomaly of macula
Focal facial dermal dysplasia 2 Brauer Setleis type
Anhidrotic, Ectodermal Dysplasia
Neonatal tooth
Autosomal dominant KID (keratitis, ichthyosis, deafness) syndrome
Zlotogora Zilberman Tenenbaum syndrome
Contracture with ectodermal dysplasia and orofacial cleft syndrome
AEC syndrome
Congenital hypotrichosis
FFDD type 4 - focal facial dermal dysplasia type 4
ANN - Anonychia
Blepharo-cheilo-odontic syndrome
Clefting, ectropion, conical teeth syndrome
Dominant autosomal hereditary disorder, incomplete penetrance
Focal facial dermal dysplasia type III
Dermotrichic syndrome
Sabinas brittle hair syndrome
Congenital absent nails
Ectodermal Dysplasias, Anhidrotic
Ectodermal dysplasia
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
Cranioectodermal dysplasia
Pilodental dysplasia, refractive errors syndrome
Hypotrichosis congenita
Nail dystrophy, deafness syndrome
Schinzel-Giedion syndrome
Sensenbrenner's syndrome
Berlin syndrome
EEM syndrome
Ectodermal dysplasia trichoodontoonychial type
Weyers acrofacial dysostosis
Hypohidrotic ectodermal dysplasia syndrome
Weyers acrodental dysostosis
Ankyloblepharon-ectodermal dysplasia-clefting syndrome
Hypohidrotic ectodermal dysplasia with immune deficiency
Elsching syndrome
Odontotrichoungual-digital-palmar syndrome
Cleft lip and cleft palate with ectodermal dysplasia syndrome
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB gain of function mutation
Anhydrotic Ectodermal Dysplasias
Acanthosis nigricans
KID syndrome
Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome
Robinson nail dystrophy-deafness syndrome
BRESEK (brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia) syndrome
Ectodermal dysplasia-ocular malformation syndrome
Odonto-tricho-ungual-digito-palmar syndrome
Hypoplasia of breast
Ectodermal dysplasia with hair-nail defect
Roselli-Gulienetti ectodermal dysplasia
Anhidrotic Ectodermal Dysplasias
Acrofacial dysostosis Weyers type
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome
Keratitis ichthyosis deafness syndrome
Hyperpigmentation of oral mucosa
Ectodermal syndrome with hair-tooth-sweating defects
Anhidrotic ectodermal dysplasia with immunodeficiency
Hypoplastic breast
Congenital hypoplasia of nail unit
Dysplasia, Anhydrotic Ectodermal
Ectodermal dysplasia and sensorineural deafness syndrome
Kopysc Barczyk Krol syndrome
Odonto onycho dysplasia with alopecia syndrome
Focal facial dermal dysplasia type IV
Keratitis, ichthyosis, deafness/hystrix-like ichthyosis deafness syndrome
TDO - Trichodento-osseous syndrome
Ectodermal dysplasia with hair-tooth defects
Trichodysplasia with amelogenesis imperfecta syndrome
Anhidrotic ectodermal dysplasia syndrome
Lelis syndrome
Congenital hypotrichia
Ectodermal dysplasia syndactyly syndrome
Trichothiodystrophy
Odonto-tricho-ungual-digito-palmar syndrome Mendoza-Valiente type
Ectodermal dysplasia, anhidrotic
Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia
Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome
Hay-Wells syndrome
Hay-Wells syndrome of ectodermal dysplasia
Robinson's syndrome
Arthrogryposis and ectodermal dysplasia syndrome
FFDD type 1 - focal facial dermal dysplasia type 1
Fried's tooth and nail syndrome
Ectodermal dysplasia with tooth-nail-sweating defect
Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes
Odonto-onycho-dermal dysplasia
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
RHOA (ras homolog family member A) related mosaic ectodermal dysplasia
Sandman-Andra syndrome
Dysplasias, Anhydrotic Ectodermal
Oligohidrosis
Ectodermal Dysplasia Anhidrotic
Euhidrotic ectodermal dysplasia
Trichoodontoonychial dysplasia
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome
Anonychia with bizarre flexural pigmentation
Fleck syndrome
Taurodontism - curly hair - osteosclerosis syndrome
Focal facial dermal dysplasia type I
RHOA-related mosaic ectodermal dysplasia
Odontomicronychial ectodermal dysplasia
Blepharocheilodontic syndrome
OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema) syndrome
Ectodermal dysplasia with sweating defect
Premature tooth eruption
Tricho-dento-osseous syndrome
X-linked mental retardation Reish type
EEM (ectodermal dysplasia, ectrodactyly, macular dystrophy) syndrome
Trichodermodysplasia and dental alterations syndrome
Accelerated tooth eruption
Ectodermal dysplasia, syndactyly and pili torti
Anonychia
Bitemporal aplasia cutis congenita
BRESEK syndrome
Limb mammary syndrome
Trichothiodystrophy type G
Cerebellar ataxia co-occurrent with ectodermal dysplasia
Focal facial preauricular dysplasia
Ackerman syndrome
Onycho-tricho-dysplasia neutropenia syndrome
Dysplasias, Anhidrotic Ectodermal
Johanson-Blizzard syndrome
Focal facial dermal dysplasia
Ectodermal dysplasia with nail defect
Ectodermal dysplasia with tooth-sweating defect
Anhydrotic Ectodermal Dysplasia
Dermo odontodysplasia
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA GOF (gain of function) mutation
Zlotogora Ogur syndrome
Ectodermal dysplasia with acanthosis nigricans syndrome
Stoll Alembik Finck syndrome
Focal facial dermal dysplasia type II
Keratitis ichthyosis and deafness syndrome
Marshall's syndrome
Rapp-Hodgkin type of ectodermal dysplasia
Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome
Amelo-onycho-hypohidrotic syndrome
Hypohydrosis
Ectodermal dysplasia with hair-tooth-nail-sweating defect
Curry-Hall syndrome
Anhidrotics, Ectodermal Dysplasia
Trichoodontoonychial dysplasia with bone deficiency in frontoparietal region
Short stature, nail dysplasia, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome
KID/HID syndrome
Ectodermal dysplasia with hair-tooth-nail defects
Ectodermal dysplasia short stature syndrome
Amelogenesis imperfecta - osteosclerosis syndrome
FFDD type 3 - focal facial dermal dysplasia type 3
Hypohidrosis
FFDD - focal facial dermal dysplasia
Kirman syndrome
Basan syndrome
TDO syndrome
Marshall syndrome
Dysplasia, Anhidrotic Ectodermal
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB GOF mutation
Mucosal melanosis
Autosomal dominant ichthyosis
FFDD type 2 - focal facial dermal dysplasia type 2
Anhidrotic ectodermal dysplasia with immune deficiency
Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome
Ectodermal dysplasia with natal teeth Turnpenny type
Setleis syndrome
Odonto-onychial dysplasia with alopecia
Ameloonychohypohidrotic syndrome
Brauer syndrome
Ladda Zonana Ramer syndrome
Congenital hypoplasia of breast
Melanin pigmentation of oral mucosa
Ectodermal syndrome with hair-sweating defects
Trichodento-osseous syndrome
Ectodermal dysplasia with tooth-nail defects
Hypohidrotic X-linked ectodermal dysplasia
Ectodermal Dysplasia, Anhydrotic
Tricho-onychodental dysplasia
Precocious dentition

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.

How does Q82.4 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like ectodermal dysplasia (anhidrotic) affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q82.4?

Q82.4 maps to the ICD-11 code: LD27.02 (Hypohidrotic ectodermal dysplasia).

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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.