Name: Hereditary disorder of the integument
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- Hereditary disorder of the integument
- Hereditary disorder of the integument (disorder)
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Concept ID: 363185004- Hereditary disorder of the integument (disorder)
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ICD-10 Codes: #HLT
- Absence of fingerprints with congenital milia syndrome (disorder)
- Acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome
- Ackerman syndrome (disorder)
- Acral dystrophic epidermolysis bullosa (disorder)
- Acral peeling skin syndrome (disorder)
- Acro-dermato-ungual-lacrimal-tooth syndrome (disorder)
- Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder)
- Alopecia and intellectual disability syndrome (disorder)
- Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
- Alopecia, contracture, dwarfism, intellectual disability syndrome (disorder)
- Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
- Alopecia, psychomotor epilepsy, periodontal pyorrhoea, intellectual disability syndrome
- Amaurosis hypertrichosis syndrome
- Ameloonychohypohidrotic syndrome (disorder)
- Anhidrotic ectodermal dysplasia with immune deficiency
- Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema syndrome
- Ankylosing vertebral hyperostosis with tylosis syndrome (disorder)
- Anonychia with microcephaly syndrome (disorder)
- Aplasia cutis congenita with epibulbar dermoid syndrome
- Aplasia cutis congenita with intestinal lymphangiectasia syndrome
- Aplasia cutis with myopia syndrome (disorder)
- Ataxia-telangiectasia syndrome
- Atrophoderma vermiculatum (disorder)
- Atypical mole syndrome (disorder)
- Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder)
- + Autosomal dominant epidermolysis bullosa simplex
- Autosomal dominant familial woolly hair (disorder)
- Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
- + Autosomal dominant mutilating keratoderma (disorder)
- Autosomal dominant palmoplantar keratoderma and congenital alopecia (disorder)
- Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome (disorder)
- Autosomal recessive popliteal pterygium syndrome (disorder)
- Bamforth Lazarus syndrome
- + Basal epidermolysis bullosa simplex (disorder)
- Blepharocheilodontic syndrome
- Book syndrome
- Brachymorphism with onychodysplasia and dysphalangism syndrome (disorder)
- Brooke-Spiegler syndrome
- Bullous dystrophy macular type
- CAMOS syndrome
- Capillary malformation-arteriovenous malformation syndrome
- Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder)
- Cervical hypertrichosis and peripheral neuropathy syndrome
- + Cholestanol storage disease (disorder)
- Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (disorder)
- Conductive deafness, ptosis, skeletal anomalies syndrome
- Congenital cataract with hypertrichosis and intellectual disability syndrome
- + Congenital ichthyosis of skin (disorder)
- Congenital lethal erythroderma
- Congenital reticular ichthyosiform erythroderma
- Contracture with ectodermal dysplasia and orofacial cleft syndrome (disorder)
- Cooks syndrome
- Crouzon syndrome with acanthosis nigricans (disorder)
- Curly hair, acral keratoderma, caries syndrome
- Cutaneous photosensitivity and lethal colitis syndrome (disorder)
- Cutis gyrata syndrome of Beare and Stevenson (disorder)
- Cutis laxa, autosomal dominant (disorder)
- + Cutis laxa, autosomal recessive (disorder)
- + Darier disease
- Deafness, enamel hypoplasia, nail defect syndrome
- Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder)
- Dermatoleukodystrophy (disorder)
- Dermatoosteolysis Kirghizian type
- Dermo-odonto dysplasia (disorder)
- Diffuse palmoplantar keratoderma and acrocyanosis syndrome (disorder)
- Disseminated superficial porokeratosis (disorder)
- + Dyskeratosis congenita
- Dystrophic epidermolysis bullosa nails only (disorder)
- Ectodermal dysplasia and sensorineural deafness syndrome (disorder)
- Ectodermal dysplasia trichoodontoonychial type (disorder)
- Ectodermal dysplasia with acanthosis nigricans syndrome (disorder)
- Ectodermal dysplasia with blindness syndrome
- Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome (disorder)
- Ectodermal dysplasia with natal teeth Turnpenny type
- Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome
- + Ehlers-Danlos syndrome
- Epidermodysplasia verruciformis (disorder)
- Epidermolysis bullosa simplex due to plakophilin deficiency
- Epidermolysis bullosa simplex with pyloric atresia
- Erythema palmare hereditarium (disorder)
- Fabry's disease
- Familial acantholysis
- Familial amyloid polyneuropathy with cutaneous amyloidosis
- Familial cold urticaria
- Familial dyskeratotic comedones (disorder)
- Familial isolated trichomegaly (disorder)
- Familial malignant melanoma of skin (disorder)
- Familial multiple fibrofolliculoma
- Farber's lipogranulomatosis (disorder)
- Focal palmoplantar and gingival keratoderma
- Follicular atrophoderma and basal cell epitheliomata
- Frontonasal dysplasia with alopecia and genital anomaly syndrome (disorder)
- Generalised peeling skin syndrome
- Generalized basaloid follicular hamartoma syndrome (disorder)
- + Genetic disorder of skin pigmentation (disorder)
- + Genetic lipodystrophy (disorder)
- Gingival fibromatosis and hypertrichosis syndrome (disorder)
- Glomuvenous malformation (disorder)
- Gorlin syndrome (disorder)
- Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder)
- Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification (disorder)
- Haim Munk syndrome
- Hair defect with photosensitivity and intellectual disability syndrome (disorder)
- Hennekam Beemer syndrome
- Hereditary acrodermatitis enteropathica
- Hereditary anetoderma
- Hereditary benign intraepithelial dyskeratosis
- + Hereditary hypotrichosis simplex
- Hereditary hypotrichosis with recurrent skin vesicles syndrome
- Hereditary keratoacanthoma (disorder)
- Hereditary neurocutaneous angiomata (disorder)
- Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder)
- + Hereditary sclerosing poikiloderma
- Hereditary skin fragility (disorder)
- Hidrotic ectodermal dysplasia Halal type
- Hirschsprung disease with nail hypoplasia and dysmorphism
- Hypertrichosis and acromegaloid facial appearance syndrome (disorder)
- Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome
- Hypohidrosis due to genetic abnormality of eccrine gland structure and function
- Hypohidrotic X-linked ectodermal dysplasia
- Hypotrichosis and intellectual disability syndrome Lopes type
- Hypotrichosis with juvenile macular degeneration syndrome (disorder)
- Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome (disorder)
- Incontinentia pigmenti syndrome (disorder)
- Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome (disorder)
- Isolated anterior cervical hypertrichosis (disorder)
- Isolated congenital adermatoglyphia (disorder)
- Johnson neuroectodermal syndrome (disorder)
- Joubert syndrome with orofaciodigital defect (disorder)
- Junctional epidermolysis bullosa non-Herlitz type (disorder)
- Keratosis follicularis, dwarfism, cerebral atrophy syndrome
- Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome (disorder)
- Kohlschutter's syndrome (disorder)
- Laryngo-onycho-cutaneous syndrome
- Late-onset junctional epidermolysis bullosa (disorder)
- Limb mammary syndrome
- Lipid proteinosis
- Lymphoedema hypoparathyroidism syndrome
- Macrostomia, preauricular tag, external ophthalmoplegia syndrome
- MACS syndrome
- Mammary digital nail syndrome (disorder)
- Mandibuloacral dysostosis (disorder)
- Melanoma and neural system tumour syndrome
- Menkes kinky-hair syndrome
- Microphthalmia with linear skin defect syndrome (disorder)
- Multiple lentigines syndrome
- Multiple self-healing epithelioma of Ferguson-Smith
- Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome
- Nail-patella syndrome (disorder)
- + Neurofibromatosis syndrome
- Non-androgenic hypertrichosis co-occurrent and due to genetic disease (disorder)
- Noonan syndrome-like disorder with loose anagen hair (disorder)
- Oculoosteocutaneous syndrome (disorder)
- Oculotrichodysplasia
- Odonto-tricho-ungual-digito-palmar syndrome
- Oliver McFarlane syndrome
- Oro-facial digital syndrome type 1 (disorder)
- Oro-facial digital syndrome type 14
- Oro-facial digital syndrome type 5
- Oro-facial digital syndrome type 8
- Oro-facial digital syndrome type 9 (disorder)
- Osler hemorrhagic telangiectasia syndrome (disorder)
- Osteopenia, intellectual disability, sparse hair syndrome (disorder)
- Oto-onycho-peroneal syndrome (disorder)
- Pachydermoperiostosis syndrome
- Palmoplantar keratoderma Nagashima type
- Palmoplantar keratoderma with clinodactyly syndrome (disorder)
- Palmoplantar keratoderma with deafness syndrome (disorder)
- Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome
- Papillon-Lefèvre syndrome (disorder)
- Pili torti onychodysplasia syndrome
- Pili torti-deafness syndrome
- Porokeratosis plantaris palmaris et disseminata
- + Premature aging syndrome (disorder)
- Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder)
- + PTEN hamartoma tumour syndrome
- Pterygium colli with intellectual disability and digital anomaly syndrome (disorder)
- Punctate palmoplantar keratoderma type 1
- Punctate palmoplantar keratoderma type 2 (disorder)
- Pyogenic arthritis, pyoderma gangrenosum, acne syndrome
- Recessive aplasia cutis congenita of limbs
- + Recessive dystrophic epidermolysis bullosa
- Rombo syndrome
- Rothmund-Thomson syndrome
- Scalp, ear, nipple syndrome (disorder)
- SCARF syndrome
- Schinzel-Giedion syndrome
- Scholte syndrome
- Sensorineural hearing loss, early greying, essential tremor syndrome
- Severe achondrolasia with developmental delay and acanthosis nigricans (disorder)
- Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder)
- Short stature with webbed neck and congenital heart disease syndrome
- Short tarsus with absence of lower eyelashes syndrome
- Sitosterolaemia with xanthomatosis
- Sparse hair with short stature and skin anomaly syndrome (disorder)
- Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder)
- Spinocerebellar ataxia type 34
- + Steatocystoma multiplex (disorder)
- Stern Lubinsky Durrie syndrome (disorder)
- Striate palmoplantar keratoderma
- Taurodontia with absent teeth and sparse hair syndrome (disorder)
- Temple Baraitser syndrome (disorder)
- Transient bullous dermolysis of newborn
- Trichodysplasia with amelogenesis imperfecta syndrome
- Trichodysplasia xeroderma syndrome (disorder)
- Trichoodontoonychial dysplasia (disorder)
- + Trichothiodystrophy (disorder)
- + Tuberous sclerosis syndrome
- Ultraviolet sensitive syndrome
- Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome (disorder)
- Upshaw-Schulman syndrome
- Van den Bosch syndrome
- Von Hippel-Lindau syndrome (disorder)
- White forelock with malformations syndrome
- Wiedemann Steiner syndrome (disorder)
- Woolly hair with palmoplantar keratoderma syndrome
- Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome (disorder)
- X-linked intellectual disability with seizure and psoriasis syndrome (disorder)
- Zlotogora Ogur syndrome