SE-ATLAS

Johanson-Blizzard syndrome Hereditary hypotrichosis with recurrent skin vesicles Ulerythema ophryogenesis Keratinopathic ichthyosis Papillon-Lefèvre syndrome Chronic cutaneous lupus erythematosus MEDNIK syndrome Primary cutaneous lymphoma Extranodal nasal NK/T cell lymphoma Primary cutaneous marginal zone B-cell lymphoma Malignant atrophic papulosis Acrofacial dysostosis, Weyers type Johnson neuroectodermal syndrome Infantile digital fibromatosis Focal palmoplantar keratoderma Limited systemic sclerosis Autosomal ichthyosis syndrome with fatal disease course Brain-lung-thyroid syndrome CREST syndrome Ectodermal dysplasia-pili torti-cutaneous syndactyly syndrome Peeling skin syndrome Genetic porokeratosis EEC syndrome and related disorders FLOTCH syndrome Primary cutaneous gamma/delta-positive T-cell lymphoma Infantile myofibromatosis Hyperkeratosis lenticularis perstans Ectodermal dysplasia-hyperhidrosis-cutaneous syndactyly syndrome Primary cutaneous follicle center lymphoma Genetic hair anomaly Flynn-Aird syndrome Systemic sclerosis Genetic epidermal appendage anomaly Rare nevus Autosomal recessive palmoplantar keratoderma and congenital alopecia Lymphedema Dyskeratosis congenita CHILD syndrome Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome Taurodontia-absent teeth-sparse hair syndrome Primary cutaneous peripheral T-cell lymphoma not otherwise specified Autosomal dominant multiple pterygium syndrome Barber-Say syndrome Autosomal ichthyosis syndrome with prominent neurologic signs LMNA-related cardiocutaneous progeria syndrome Subcutaneous panniculitis-like T-cell lymphoma Typical urticaria pigmentosa White sponge nevus Peutz-Jeghers syndrome Rare skin tumor or hamartoma Hypotrichosis simplex Familial multiple lipomatosis Angora hair nevus Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome Genetic nail anomaly Epidermolysis bullosa simplex with anodontia/hypodontia Primary cutaneous diffuse large B-cell lymphoma, leg type Unclassified genetic skin disorder Bartsocas-Papas syndrome Isolated focal palmoplantar keratoderma Generalized eruptive keratoacanthoma Van den Bosch syndrome Multiple self-healing squamous epithelioma Disease with diffuse palmoplantar keratoderma as a major feature Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome Familial angiolipomatosis Tyrosinemia type 2 Autosomal ichthyosis syndrome with other associated signs Phakomatosis pigmentokeratotica Nodular urticaria pigmentosa Indolent primary cutaneous T-cell lymphoma Premature aging Phakomatosis pigmentovascularis Cataract-hypertrichosis-intellectual disability syndrome Hypertrichosis-acromegaloid facial appearance syndrome Autosomal dominant isolated diffuse palmoplantar keratoderma Gardner syndrome Plaque-form urticaria pigmentosa Hypermobile Ehlers-Danlos syndrome Systemic mastocytosis Epidermolysis bullosa simplex due to BP230 deficiency Malignant melanoma of the mucosa Scleromyxedema Rare genetic skin disease Autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature Vascular Ehlers-Danlos syndrome Congenital ichthyosiform erythroderma Smoldering systemic mastocytosis Genetic pigmentation anomaly of the skin Classical Ehlers-Danlos syndrome Dermatofibrosarcoma protuberans Marshall syndrome Nestor-Guillermo progeria syndrome Genetic sebaceous gland anomaly Cranioectodermal dysplasia Kein Name gefunden Parkes Weber syndrome ANE syndrome Autosomal dominant generalized epidermolysis bullosa simplex, severe form Self-improving collodion baby Palmoplantar keratoderma-esophageal carcinoma syndrome Klippel-Trénaunay syndrome Autoimmune bullous skin disease Autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature Ellis Van Creveld syndrome Aggressive primary cutaneous T-cell lymphoma Keratoderma hereditarium mutilans with ichthyosis McCune-Albright syndrome Epidermolytic palmoplantar keratoderma Genetic hyperpigmentation of the skin Epidermolysis bullosa simplex due to exophilin 5 deficiency Teebi-Shaltout syndrome Autosomal recessive disease with focal palmoplantar keratoderma as a major feature Focal palmoplantar and gingival keratoderma Diffuse palmoplantar keratoderma, Bothnian type Indolent primary cutaneous B-cell lymphoma Epidermolysis bullosa simplex with mottled pigmentation Alopecia totalis Palmoplantar keratoderma-spastic paralysis syndrome Autosomal recessive isolated diffuse palmoplantar keratoderma Ehlers-Danlos syndrome type 1 Palmoplantar keratoderma-deafness syndrome Isolated punctate palmoplantar keratoderma Localized epidermolysis bullosa simplex Dermatitis herpetiformis Alopecia universalis Aggressive primary cutaneous B-cell lymphoma PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement Linear verrucous nevus syndrome Piebaldism Primary non-essential cutis verticis gyrata Isolated bone marrow mastocytosis Keratosis follicularis-dwarfism-cerebral atrophy syndrome Didymosis aplasticosebacea Dermatoosteolysis, Kirghizian type Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form Linear nevus sebaceus syndrome GAPO syndrome Trichorhinophalangeal syndrome Keratosis follicularis spinulosa decalvans Absence of fingerprints-congenital milia syndrome LUMBAR syndrome Bullous pemphigoid Piebald trait-neurologic defects syndrome Syndromic oculocutaneous albinism SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome Syringocystadenoma papilliferum Orofaciodigital syndrome type 1 Pemphigus vulgaris Junctional epidermolysis bullosa with pyloric atresia Aplasia cutis congenita Trichodysplasia-amelogenesis imperfecta syndrome PTEN hamartoma tumor syndrome Minimal pigment oculocutaneous albinism type 1 Nail-patella syndrome Exfoliative ichthyosis Sebocystomatosis ADULT syndrome Haim-Munk syndrome Porokeratotic eccrine ostial and dermal duct nevus Localized junctional epidermolysis bullosa Intermediate generalized junctional epidermolysis bullosa Dermoodontodysplasia Recessive aplasia cutis congenita of limbs Xeroderma pigmentosum-Cockayne syndrome complex Congenital panfollicular nevus Sparse hair-short stature-skin anomalies syndrome NEVADA syndrome Temperature-sensitive oculocutaneous albinism type 1 Junctional epidermolysis bullosa inversa Aplasia cutis congenita-intestinal lymphangiectasia syndrome Sézary syndrome Genetic hypopigmentation of the skin Pili torti Ehlers-Danlos syndrome type 2 Severe generalized junctional epidermolysis bullosa Aplasia cutis-myopia syndrome Familial isolated trichomegaly SCALP syndrome Neurocutaneous melanocytosis Ito hypomelanosis Pili torti-onychodysplasia syndrome Oculocutaneous albinism type 1 Focal facial dermal dysplasia type I Pili torti-developmental delay-neurological abnormalities syndrome Angioosteohypertrophic syndrome Late-onset junctional epidermolysis bullosa Monilethrix Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency Pilodental dysplasia-refractive errors syndrome Marginal papular palmoplantar keratoderma Hereditary coproporphyria Recessive dystrophic epidermolysis bullosa inversa Megalencephaly-capillary malformation-polymicrogyria syndrome Seborrhea-like dermatitis with psoriasiform elements Acral self-healing collodion baby Familial atypical multiple mole melanoma syndrome Acral peeling skin syndrome Primary cutaneous B-cell lymphoma Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form Muckle-Wells syndrome Meige disease Chédiak-Higashi syndrome Cockayne syndrome type 2 Pilomatrixoma Dystrophic epidermolysis bullosa Waardenburg syndrome Self-improving dystrophic epidermolysis bullosa Epidermolysis bullosa simplex Localized dystrophic epidermolysis bullosa, pretibial form Genetic dermis elastic tissue disorder Non-hereditary late-onset primary lymphedema Lymphoadenopathic mastocytosis with eosinophilia Loose anagen syndrome Cockayne syndrome type 1 Disease with focal palmoplantar keratoderma as a major feature Geroderma osteodysplastica Cutaneous neuroendocrine carcinoma Junctional epidermolysis bullosa Ringed hair disease Mycosis fungoides and variants Congenital erythropoietic porphyria Annular epidermolytic ichthyosis Genetic skin vascular disorder Hereditary painful callosities Pityriasis rubra pilaris Woolly hair Cockayne syndrome type 3 Acute intermittent porphyria Ehlers-Danlos syndrome with periventricular heterotopia Focal facial dermal dysplasia type III Classic mast cell leukemia Oculocutaneous albinism type 7 Progressive osseous heteroplasia Paraneoplastic pemphigus Böök syndrome Isolated congenital anonychia Hereditary poikiloderma Marie Unna hereditary hypotrichosis Hidrotic ectodermal dysplasia, Christianson-Fourie type Woolly hair nevus Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome Cervical hypertrichosis-peripheral neuropathy syndrome Genetic mixed dermis disorder Genetic subcutaneous tissue disorder Autosomal erythropoietic protoporphyria Ehlers-Danlos syndrome type 7B Hidrotic ectodermal dysplasia, Halal type Suprabasal epidermolysis bullosa simplex Tricho-retino-dento-digital syndrome Dowling-Degos disease Keratosis palmaris et plantaris-clinodactyly syndrome Amelocerebrohypohidrotic syndrome Autosomal dominant hypohidrotic ectodermal dysplasia Hypertrichosis cubiti Generalized peeling skin syndrome Ehlers-Danlos syndrome type 7A Odontomicronychial dysplasia Acrokeratoelastoidosis of Costa Onychocytic matricoma Pili bifurcati Diffuse palmoplantar keratoderma-acrocyanosis syndrome Cartilage-hair hypoplasia Isolated congenital onychodysplasia Familial reactive perforating collagenosis Autosomal dominant epidermolytic ichthyosis Linear atrophoderma of Moulin Anonychia congenita totalis Hypertrichosis lanuginosa congenita Dermatopathia pigmentosa reticularis Basal epidermolysis bullosa simplex Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Familial progressive hyperpigmentation Lamellar ichthyosis Dyschromatosis symmetrica hereditaria Acroosteolysis-keloid-like lesions-premature aging syndrome Dermochondrocorneal dystrophy Rare nail tumor Hereditary palmoplantar keratoderma, Gamborg-Nielsen type Primary lymphedema Muir-Torre syndrome Aleukemic mast cell leukemia AREDYLD syndrome Erythrokeratoderma ''en cocardes Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome Hereditary acrokeratotic poikiloderma Ectodermal dysplasia-skin fragility syndrome Acrokeratosis verruciformis of Hopf Progressive symmetric erythrokeratodermia Albinism-deafness syndrome Linear and whorled nevoid hypermelanosis Focal facial dermal dysplasia Kindler epidermolysis bullosa Erythrokeratodermia variabilis Hair defect-photosensitivity-intellectual disability syndrome Chondroectodermal dysplasia with night blindness X-linked hypohidrotic ectodermal dysplasia Lacrimoauriculodentodigital syndrome Congenital lethal erythroderma Hermansky-Pudlak syndrome due to BLOC-3 deficiency Reticulate acropigmentation of Kitamura Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome Acrogeria Acquired ichthyosis Bathing suit ichthyosis Ectodermal dysplasia, trichoodontoonychial type Rothmund-Thomson syndrome Idiopathic trachyonychia Wiedemann-Rautenstrauch syndrome Focal acral hyperkeratosis Trichofolliculoma Spinocerebellar ataxia type 34 Hypodontia-dysplasia of nails syndrome Superficial epidermolytic ichthyosis Onychomatricoma Lelis syndrome Focal dermal hypoplasia Disseminated superficial actinic porokeratosis Uncombable hair syndrome Diffuse lymphatic malformation Genetic photodermatosis Erythromelalgia Steatocystoma multiplex-natal teeth syndrome Lipedema Disease with punctate palmoplantar keratoderma as a major feature Localized dystrophic epidermolysis bullosa, acral form Harlequin ichthyosis Ehlers-Danlos syndrome Scalp defects-postaxial polydactyly syndrome Gorlin-Chaudhry-Moss syndrome Hermansky-Pudlak syndrome Familial multiple trichoepithelioma Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome Xeroderma pigmentosum variant Multiple benign circumferential skin creases on limbs Alopecia-contractures-dwarfism-intellectual disability syndrome Primary cutaneous T-cell lymphoma Oculocutaneous albinism type 2 Osteopathia striata-pigmentary dermopathy-white forelock syndrome Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies Alopecia antibody deficiency Recessive X-linked ichthyosis Oculocutaneous albinism type 1A Hidrotic ectodermal dysplasia Nevus of Ota Porokeratosis of Mibelli Rothmund-Thomson syndrome type 1 Focal facial dermal dysplasia type II Alopecia-epilepsy-pyorrhea-intellectual disability syndrome Cockayne syndrome Familial normophosphatemic tumoral calcinosis Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome Oculocutaneous albinism type 3 Oculocutaneous albinism type 4 CLOVES syndrome Generalized basaloid follicular hamartoma syndrome Incontinentia pigmenti Oculocutaneous albinism Oculocutaneous albinism type 1B Porokeratosis plantaris palmaris et disseminata Severe achondroplasia-developmental delay-acanthosis nigricans syndrome Autosomal dominant cutis laxa Localized dystrophic epidermolysis bullosa, nails only Autosomal dominant palmoplantar keratoderma and congenital alopecia Skin fragility-woolly hair-palmoplantar keratoderma syndrome Cutis marmorata telangiectatica congenita Epidermolysis bullosa simplex with circinate migratory erythema Oculocutaneous albinism type 5 Porphyria Juvenile xanthogranuloma Corneodermatoosseous syndrome Autosomal recessive cutis laxa type 2 Hutchinson-Gilford progeria syndrome Focal facial dermal dysplasia type IV Autosomal recessive cutis laxa type 1 Hermansky-Pudlak syndrome due to BLOC-2 deficiency Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome Hypohidrotic ectodermal dysplasia Congenital smooth muscle hamartoma Farber disease RIN2 syndrome Occipital horn syndrome Rothmund-Thomson syndrome type 2 Trichorhinophalangeal syndrome type 1 Proteus syndrome Hallermann-Streiff syndrome Brittle cornea syndrome Dahlberg-Borer-Newcomer syndrome Nevus of Ito Erythrokeratoderma variabilis progressiva Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering Autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature Epidermolysis bullosa simplex with pyloric atresia Isolated congenital digital clubbing CHIME syndrome Cowden syndrome Familial multiple fibrofolliculoma Hypohidrotic ectodermal dysplasia with immunodeficiency Autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature ALDH18A1-related De Barsy syndrome Crandall syndrome Toriello-Lacassie-Droste syndrome Cronkhite-Canada syndrome Familial progressive hyper- and hypopigmentation Classical-like Ehlers-Danlos syndrome type 1 Odonto-tricho-ungual-digito-palmar syndrome Cleft lip/palate-ectodermal dysplasia syndrome Lethal acantholytic erosive disorder Leukoencephalopathy-palmoplantar keratoderma syndrome Striate palmoplantar keratoderma Leukonychia totalis KID syndrome Pachydermoperiostosis Arterial tortuosity syndrome Keratolytic winter erythema Congenital generalized hypertrichosis, Ambras type Choroidal atrophy-alopecia syndrome Pure hair and nail ectodermal dysplasia Non-hereditary congenital primary lymphedema Schöpf-Schulz-Passarge syndrome Hartnup disease Ectodermal dysplasia with natal teeth, Turnpenny type Frontonasal dysplasia-alopecia-genital anomalies syndrome Oculocutaneous albinism type 6 Vascular-like classical Ehlers-Danlos syndrome B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome CEDNIK syndrome X-linked reticulate pigmentary disorder Milroy disease Limb-mammary syndrome Curly hair-acral keratoderma-caries syndrome Hereditary acrokeratotic poikiloderma of Kindler-Weary Familial melanoma Cutis laxa Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Hypotrichosis with juvenile macular degeneration UV-sensitive syndrome Epidermal nevus syndrome Amelo-onycho-hypohidrotic syndrome Hermansky-Pudlak syndrome due to BLOC-1 deficiency X-linked Ehlers-Danlos syndrome Atrichia with papular lesions Naegeli-Franceschetti-Jadassohn syndrome Familial cylindromatosis Diffuse cutaneous mastocytosis Ehlers-Danlos syndrome, fibronectinemic type Mal de Meleda Palmoplantar keratoderma, Nagashima type Pseudoxanthoma elasticum Waardenburg syndrome type 1 Cutaneous mastocytoma Waardenburg syndrome type 2 Deaf blind hypopigmentation syndrome, Yemenite type Oley syndrome Pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome Trichodental syndrome Encephalocraniocutaneous lipomatosis Waardenburg syndrome type 3 Hypotrichosis simplex of the scalp Tricho-dento-osseous syndrome Buschke-Ollendorff syndrome Autosomal dominant diffuse mutilating palmoplantar keratoderma Maculopapular cutaneous mastocytosis Familial multiple nevi flammei Multiple symmetric lipomatosis Trichodermodysplasia-dental alterations syndrome Cardiac-valvular Ehlers-Danlos syndrome Follicular atrophoderma-basal cell carcinoma Large congenital melanocytic nevus Tricho-oculo-dermo-vertebral syndrome Darier disease Trichoodontoonychial dysplasia Hypopigmentation-punctate palmoplantar keratoderma syndrome Hereditary sclerosing poikiloderma, Weary type Craniofaciofrontodigital syndrome Proliferating trichilemmal cyst Deafness-enamel hypoplasia-nail defects syndrome Congenital reticular ichthyosiform erythroderma Hemihyperplasia-multiple lipomatosis syndrome Werner syndrome Ehlers-Danlos/osteogenesis imperfecta syndrome Familial keratoacanthoma Hermansky-Pudlak syndrome type 8 Parana hard skin syndrome Dermatomyositis Trichothiodystrophy Full schwannomatosis Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome Cutaneous mastocytosis Transgrediens et progrediens palmoplantar keratoderma Verrucous nevus Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Carvajal syndrome Inflammatory linear verrucous epidermal nevus Blepharo-cheilo-odontic syndrome Laryngo-onycho-cutaneous syndrome Netherton syndrome Musculocontractural Ehlers-Danlos syndrome Trichomegaly-retina pigmentary degeneration-dwarfism syndrome Acanthokeratolytic verrucous nevus Fanconi anemia Ichthyosis follicularis-alopecia-photophobia syndrome Trichodysplasia-xeroderma syndrome Erythropoietic uroporphyria associated with myeloid malignancy Autosomal dominant trichoodontoonychodysplasia-syndactyly Keratosis pilaris atrophicans Generalized pustular psoriasis Neurofibromatosis type 1 Full NF2-related schwannomatosis PASH syndrome Poikiloderma with neutropenia Mastocytosis Xeroderma pigmentosum Porphyria variegata Epidermolysis bullosa simplex superficialis Autosomal recessive nail dysplasia Trichorhinophalangeal syndrome type 2 Autosomal recessive generalized epidermolysis bullosa simplex Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome Acute hepatic porphyria Deafness-onychodystrophy syndrome Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Hereditary bullous dystrophy, macular type Centripetalis recessive dystrophic epidermolysis bullosa Progeria-short stature-pigmented nevi syndrome Rare systemic or rheumatologic disease Junctional epidermolysis bullosa, non-Herlitz type Graham Little-Piccardi-Lassueur syndrome Bullous diffuse cutaneous mastocytosis Atypical Werner syndrome Hepatoerythropoietic porphyria Rare lymphatic malformation Griscelli syndrome type 2 Telangiectasia macularis eruptiva perstans Dystrophic epidermolysis bullosa pruriginosa Chronic hepatic porphyria Hermansky-Pudlak syndrome due to AP-3 deficiency Griscelli syndrome type 1 Pemphigus vegetans Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form De Barsy syndrome Familial anetoderma Dubowitz syndrome Progeroid syndrome, Petty type Conductive deafness-ptosis-skeletal anomalies syndrome Maffucci syndrome Griscelli syndrome type 3 Familial primary localized cutaneous amyloidosis Ataxia-telangiectasia Anonychia-onychodystrophy syndrome Systemic mastocytosis with associated hematologic neoplasm Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Diffuse palmoplantar keratoderma with painful fissures Pemphigus foliaceus Mast cell sarcoma Microphthalmia with linear skin defects syndrome Autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature Pemphigus erythematosus Hermansky-Pudlak syndrome type 9 COFS syndrome Indolent systemic mastocytosis Hypotrichosis-deafness syndrome Mast cell leukemia Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Periodontal Ehlers-Danlos syndrome Phakomatosis cesiomarmorata Aggressive systemic mastocytosis PENS syndrome Severe dermatitis-multiple allergies-metabolic wasting syndrome Granulomatous slack skin Blue rubber bleb nevus Familial cutaneous collagenoma Extracutaneous mastocytoma Neonatal inflammatory skin and bowel disease Gorlin syndrome Phakomatosis cesioflammea Pseudoxanthomatous diffuse cutaneous mastocytosis Dyschromatosis universalis hereditaria Proteus-like syndrome Nevus comedonicus syndrome Fried's tooth and nail syndrome Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome Stiff skin syndrome Cystic hygroma Pyramidal molars-abnormal upper lip syndrome Becker nevus syndrome Phakomatosis spilorosea Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome Griscelli syndrome Hyperkeratosis-hyperpigmentation syndrome Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome Bannayan-Riley-Ruvalcaba syndrome Ichthyosis Pellagra-like skin rash-neurological manifestations syndrome Rombo syndrome Palpebral sebaceous gland tumor Microcystic lymphatic malformation Noonan syndrome-like disorder with loose anagen hair Macrocystic lymphatic malformation Autosomal ichthyosis syndrome Ectodermal dysplasia-sensorineural deafness syndrome Terminal osseous dysplasia-pigmentary defects syndrome Pili gemini SAPHO syndrome Huriez syndrome Tietz syndrome Autosomal recessive hypohidrotic ectodermal dysplasia Anonychia with flexural pigmentation X-linked ichthyosis syndrome Cardiofaciocutaneous syndrome Superficial pemphigus Familial articular hypermobility syndrome Bazex-Dupré-Christol syndrome Autosomal dominant generalized dystrophic epidermolysis bullosa Epidermolysis bullosa acquisita PAPA syndrome Familial benign chronic pemphigus Isolated anterior cervical hypertrichosis Mucous membrane pemphigoid Familial tumoral calcinosis Hereditary leiomyomatosis and renal cell cancer Focal palmoplantar keratoderma with joint keratoses Linear IgA dermatosis Brooke-Spiegler syndrome Hereditary palmoplantar keratoderma Other genetic epidermal disease Autosomal ichthyosis syndrome with prominent hair abnormalities Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Cleft lip/palate-ectodermal dysplasia syndrome X-linked congenital generalized hypertrichosis Schinzel-Giedion syndrome Gingival fibromatosis-hypertrichosis syndrome Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome Herpetiform pemphigus Autosomal dominant deafness-onychodystrophy syndrome Genetic epidermal disorder Naxos disease Inherited epidermolysis bullosa Oculodentodigital dysplasia Juvenile hyaline fibromatosis Autosomal recessive cutis laxa type 2A Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma Contractures-ectodermal dysplasia-cleft lip/palate syndrome Roch-Leri mesosomatous lipomatosis Inherited non-syndromic ichthyosis Alopecia Punctate palmoplantar keratoderma type 1 Epidermolysis bullosa simplex with muscular dystrophy Legius syndrome Fibrosarcoma X-linked dominant chondrodysplasia punctata Lipoid proteinosis Undifferentiated connective tissue syndrome Birt-Hogg-Dubé syndrome Isolated hair shaft abnormality DOORS syndrome Oculoosteocutaneous syndrome Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency Diffuse cutaneous systemic sclerosis Ledderhose disease Erythema palmare hereditarium Ichthyosis hystrix of Curth-Macklin Alopecia-intellectual disability syndrome Björnstad syndrome Cooks syndrome Rare disorder with hypertrichosis EEC syndrome Antecubital pterygium syndrome Pustulosis palmaris et plantaris Dermotrichic syndrome Inherited ichthyosis syndromic form Punctate palmoplantar keratoderma type 2 PYCR1-related De Barsy syndrome H syndrome EEM syndrome Chilblain lupus Isolated nail anomaly Superficial fibromatosis Bloom syndrome Syndromic hair shaft abnormality Autosomal recessive cutis laxa type 2B Rare cutaneous lupus erythematosus Ichthyosis hystrix gravior Primary cutis verticis gyrata Arthrochalasia Ehlers-Danlos syndrome Autosomal recessive multiple pterygium syndrome Familial cold urticaria Hypertrophic or verrucous lupus erythematosus Pachyonychia congenita Autosomal recessive congenital ichthyosis Porphyria cutanea tarda Acrodermatitis continua of Hallopeau Discoid lupus erythematosus Oculotrichodysplasia Pemphigoid gestationis Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency Scalp-ear-nipple syndrome Isolated diffuse palmoplantar keratoderma Inherited ichthyosis Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome Syndromic nail anomaly Oculocerebral hypopigmentation syndrome, Cross type Punctate palmoplantar keratoderma Dermatosparaxis Ehlers-Danlos syndrome Syndromic recessive X-linked ichthyosis Lupus erythematosus tumidus Limited cutaneous systemic sclerosis Atrophoderma vermiculata Vici syndrome Ectodermal dysplasia syndrome Diffuse palmoplantar keratoderma Odonto-onycho-dermal dysplasia CLAPO syndrome Genetic acrokeratoderma Subacute cutaneous lupus erythematosus Lymphedema-distichiasis syndrome Calcifying aponeurotic fibroma Odonto-onycho dysplasia-alopecia syndrome Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma Genetic erythrokeratoderma Lupus erythematosus panniculitis Familial generalized lentiginosis Carney complex Primary cutaneous CD30+ T-cell lymphoproliferative disease Porphyria due to ALA dehydratase deficiency Odontotrichomelic syndrome Adult T-cell leukemia/lymphoma