SE-ATLAS

Keratoderma hereditarium mutilans with ichthyosis Dermatofibrosarcoma protuberans Congenital ichthyosiform erythroderma Self-improving collodion baby Aggressive primary cutaneous B-cell lymphoma Autoimmune bullous skin disease Aggressive primary cutaneous T-cell lymphoma Indolent primary cutaneous B-cell lymphoma Alopecia totalis Alopecia universalis Dermatitis herpetiformis Linear verrucous nevus syndrome Piebaldism Congenital panfollicular nevus Linear nevus sebaceus syndrome Piebald trait-neurologic defects syndrome Bullous pemphigoid Syringocystadenoma papilliferum Didymosis aplasticosebacea Pemphigus vulgaris Porokeratotic eccrine ostial and dermal duct nevus Acral peeling skin syndrome Exfoliative ichthyosis PTEN hamartoma tumor syndrome Ichthyosis-hypotrichosis syndrome Pili torti Sézary syndrome Temperature-sensitive oculocutaneous albinism type 1 Neurocutaneous melanocytosis Ito hypomelanosis NEVADA syndrome Pili torti-developmental delay-neurological abnormalities syndrome Monilethrix SCALP syndrome Mycosis fungoides and variants Oculocutaneous albinism type 1 Acral self-healing collodion baby Minimal pigment oculocutaneous albinism type 1 Primary cutaneous B-cell lymphoma Waardenburg syndrome Syndromic oculocutaneous albinism Chédiak-Higashi syndrome Loose anagen syndrome Annular epidermolytic ichthyosis Ringed hair disease Pilomatrixoma Woolly hair nevus Woolly hair Paraneoplastic pemphigus Oculocutaneous albinism type 7 Cutaneous neuroendocrine carcinoma Marie Unna hereditary hypotrichosis Osteosclerosis-ichthyosis-premature ovarian failure syndrome Cervical hypertrichosis-peripheral neuropathy syndrome Dermatopathia pigmentosa reticularis Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Familial progressive hyperpigmentation Hypertrichosis cubiti Pili bifurcati Acquired hypertrichosis lanuginosa Onychocytic matricoma Dowling-Degos disease Acromelanosis Autosomal dominant epidermolytic ichthyosis Generalized peeling skin syndrome Hypertrichosis lanuginosa congenita Lamellar ichthyosis Rare nail tumor Dyschromatosis symmetrica hereditaria Muir-Torre syndrome Linear and whorled nevoid hypermelanosis Peeling skin syndrome type A Albinism-deafness syndrome Hair defect-photosensitivity-intellectual disability syndrome Non-Langerhans cell histiocytosis Erythrokeratodermia variabilis Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome Trichofolliculoma Superficial epidermolytic ichthyosis Diffuse lymphatic malformation Uncombable hair syndrome Peeling skin syndrome type B Multicentric reticulohistiocytosis Reticulate acropigmentation of Kitamura Onychomatricoma Bathing suit ichthyosis Harlequin ichthyosis Hermansky-Pudlak syndrome due to BLOC-3 deficiency Familial multiple trichoepithelioma CLOVES syndrome Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome Peeling skin syndrome type C Oculocutaneous albinism type 1A Primary cutaneous T-cell lymphoma Alopecia antibody deficiency Hermansky-Pudlak syndrome Osteopathia striata-pigmentary dermopathy-white forelock syndrome Autoinflammatory syndrome with skin involvement PASH syndrome Recessive X-linked ichthyosis Generalized eruptive histiocytosis Hermansky-Pudlak syndrome due to BLOC-2 deficiency Oculocutaneous albinism type 3 Alopecia-epilepsy-pyorrhea-intellectual disability syndrome Oculocutaneous albinism type 2 Benign cephalic histiocytosis Systemic disease with skin involvement Oculocutaneous albinism Nevus of Ota Generalized basaloid follicular hamartoma syndrome Familial normophosphatemic tumoral calcinosis Oculocutaneous albinism type 1B Oculocutaneous albinism type 4 Juvenile xanthogranuloma Nevus of Ito Oculocutaneous albinism type 5 Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome Drug-induced lupus erythematosus Congenital smooth muscle hamartoma Proteus syndrome Xanthoma disseminatum Cowden syndrome Familial multiple fibrofolliculoma Crandall syndrome Familial progressive hyper- and hypopigmentation KID syndrome Congenital generalized hypertrichosis, Ambras type Papular xanthoma Infantile onset panniculitis with uveitis and systemic granulomatosis Naegeli-Franceschetti-Jadassohn syndrome Necrobiotic xanthogranuloma Frontonasal dysplasia-alopecia-genital anomalies syndrome Oculocutaneous albinism type 6 Familial melanoma CEDNIK syndrome Epidermal nevus syndrome Quinquaud folliculitis decalvans Familial cylindromatosis Generalized pustular psoriasis Atrichia with papular lesions Hermansky-Pudlak syndrome due to BLOC-1 deficiency Waardenburg syndrome type 1 Hypotrichosis simplex of the scalp Waardenburg syndrome type 2 Deaf blind hypopigmentation syndrome, Yemenite type Waardenburg syndrome type 3 Trichodental syndrome Follicular atrophoderma-basal cell carcinoma Hermansky-Pudlak syndrome type 8 Tricho-dento-osseous syndrome Pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome Progressive nodular histiocytosis Syndrome d'Oley Histiocytose à cellule indeterminée Naevus pigmentaire congénital géant Kyste trichilemmal proliférant Syndrome de la lipomatose multiple-hémihyperplasie Erythrodermie congénitale ichtyosiforme réticulaire Kératoacanthome familial Syndrome salt-and-pepper Syndrome d'ichtyose-joues proéminentes-sourcils latéraux Trichothiodystrophie Histiocytose progressive mucineuse héréditaire Syndrome d'ichtyose-alopécie-éclabion-ectropion-déficience intellectuelle Naevus verruqueux Naevus verruqueux acantho-kératolytique Syndrome de leuconychie totale-lésions de type acanthosis nigricans-cheveux anormaux Naevus épidermique verruqueux inflammatoire linéaire Syndrome de trichodysplasie-xérodermie Syndrome de Netherton Syndrome d'ichtyose congénitale-microcéphalie-tétraplégie Maladie d'Erdheim-Chester Syndrome d'ichtyose-doigts fusiformes-sillon labial médian Syndrome d'ichtyose folliculaire-alopécie-photophobie Syndrome d'hypotrichose-surdité Syndrome de kératose linéaire-ichtyose congénitale-kératodermie sclérosante Syndrome de Griscelli type 1 Syndrome de Graham Little-Piccardi-Lassueur Malformation lymphatique rare Syndrome de Griscelli type 3 Syndrome de Reynolds Syndrome de Hermansky-Pudlak par déficit en AP-3 Syndrome de Griscelli type 2 Pemphigus érythémateux Pemphigus végétant Syndrome de Hermansky-Pudlak type 9 Syndrome d'ichtyose-prématurité Pemphigus foliacé Syndrome PENS Syndrome du naevus comédonien Chalazodermie granulomateuse Phacomatose spilorosea Syndrome de Gorlin Syndrome Proteus-like Phacomatose cesioflammea Dyschromatose héréditaire universelle Phacomatose cesiomarmorata Syndrome du naevus de Becker Hygrome kystique Syndrome de Griscelli Syndrome d'hyperkératose-hyperpigmentation Malformation lymphatique macrokystique Syndrome de Bannayan-Riley-Ruvalcaba Syndrome de Rombo Syndrome Noonan-like avec cheveux anagènes caducs Ichtyose Malformation lymphatique microkystique Syndrome de Tietz Syndrome de Brooke-Spiegler Pemphigus superficiel Syndrome de Bazex-Dupré-Christol Syndrome PAPA Pili gemini Syndrome de dysplasie osseuse terminale-défauts de pigmentation Hypertrichose cervicale antérieure isolée Calcinose tumorale familiale Pemphigoïde des membranes muqueuses Léiomyomatose familiale et cancer du rein Hypertrichose congénitale généralisée liée à l'X Dermatose à IgA linéaire Epidermolysis bullosa acquisita Lichen plan pilaire Syndrome de fibromatose gingivale-hypertrichose Maladie de Ledderhose Syndrome de macules cutanées hypo- et hypermélaniques-retard de croissance-déficience intellectuelle Anomalie des cheveux Pemphigus herpétiforme Sclérodermie Ichtyose liée à l'X syndromique Maladie rare avec hypertrichose Chondrodysplasie ponctuée dominante liée à l'X Alopécie Syndrome de Perniola-Krajewska-Carnevale Syndrome de Birt-Hogg-Dubé Alopécie frontale fibrosante Syndrome avec anomalie de la gaine des cheveux Syndrome de Björnstad Sclérose tubéreuse de Bourneville Ichtyose hystrix gravior Ichtyose héréditaire syndromique Ichtyose syndromique autosomique avec anomalie des cheveux prédominante Anomalie isolée de la gaine des cheveux Lymphome T cutané à cellules pléomorphes de taille petite à moyenne CD4+ Sclérose systémique cutanée diffuse Ichtyose hystrix de Curth-Macklin Pemphigoïde gravidique Fibrome aponévrotique calcifié Lymphome T cutané épidermotrope CD8+ d'évolution agressive Fibromatose superficielle Ichtyose congénitale autosomique récessive Syndrome d'hypertrophie segmentaire-lipomatose-malformation artérioveineuse-naevus épidermique Syndrome oculo-cérébral d'hypopigmentation, type Cross Syndrome H Syndrome CLAPO Pseudo-pelade de Brocq Leucémie/lymphome T de l'adulte Anomalie de la pigmentation cutanée Limited cutaneous systemic sclerosis Hypopigmentation of the skin Primary cutaneous CD30+ T-cell lymphoproliferative disease Primary cutaneous lymphoma Familial generalized lentiginosis Hyperpigmentation of the skin Localized scleroderma Primary cutaneous marginal zone B-cell lymphoma Sjögren-Larsson syndrome Autosomal ichthyosis syndrome with fatal disease course Hereditary hypotrichosis with recurrent skin vesicles Infantile digital fibromatosis Extranodal nasal NK/T cell lymphoma Peeling skin syndrome Systemic sclerosis Infantile myofibromatosis Primary cutaneous gamma/delta-positive T-cell lymphoma Limited systemic sclerosis CREST syndrome MEDNIK syndrome Autosomal ichthyosis syndrome with other associated signs Primary cutaneous follicle center lymphoma Subcutaneous panniculitis-like T-cell lymphoma Rare nevus Dyskeratosis congenita CHILD syndrome Autosomal ichthyosis syndrome with prominent neurologic signs Barber-Say syndrome Keratinopathic ichthyosis Primary cutaneous peripheral T-cell lymphoma not otherwise specified Primary cutaneous diffuse large B-cell lymphoma, leg type Angora hair nevus Rare skin tumor or hamartoma Hypotrichosis simplex Multiple self-healing squamous epithelioma White sponge nevus Phakomatosis pigmentokeratotica Indolent primary cutaneous T-cell lymphoma Phakomatosis pigmentovascularis ANE syndrome Cataract-hypertrichosis-intellectual disability syndrome Hypertrichosis-acromegaloid facial appearance syndrome Malignant melanoma of the mucosa Congenital cataract-ichthyosis syndrome Gardner syndrome