SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that are treated in this facility:
ADULT syndrome ANE syndrome AREDYLD syndrome Acquired hypertrichosis lanuginosa Acral peeling skin syndrome Acral self-healing collodion baby Acrofacial dysostosis, Weyers type Alopecia Alopecia antibody deficiency Alopecia totalis Alopecia universalis Alopecia-contractures-dwarfism-intellectual disability syndrome Alopecia-epilepsy-pyorrhea-intellectual disability syndrome Alopecia-intellectual disability syndrome Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome Amelo-onycho-hypohidrotic syndrome Amelocerebrohypohidrotic syndrome Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Annular epidermolytic ichthyosis Anonychia with flexural pigmentation Atrichia with papular lesions Autosomal dominant deafness-onychodystrophy syndrome Autosomal dominant epidermolytic ichthyosis Autosomal dominant generalized dystrophic epidermolysis bullosa Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form Autosomal dominant generalized epidermolysis bullosa simplex, severe form Autosomal dominant hypohidrotic ectodermal dysplasia Autosomal dominant palmoplantar keratoderma and congenital alopecia Autosomal dominant trichoodontoonychodysplasia-syndactyly Autosomal ichthyosis syndrome with fatal disease course Autosomal ichthyosis syndrome with other associated signs Autosomal ichthyosis syndrome with prominent hair abnormalities Autosomal ichthyosis syndrome with prominent neurologic signs Autosomal recessive congenital ichthyosis Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form Autosomal recessive generalized epidermolysis bullosa simplex Autosomal recessive hypohidrotic ectodermal dysplasia Autosomal recessive palmoplantar keratoderma and congenital alopecia Barber-Say syndrome Bartsocas-Papas syndrome Basal epidermolysis bullosa simplex Bathing suit ichthyosis Björnstad syndrome Blepharo-cheilo-odontic syndrome Böök syndrome CEDNIK syndrome CHILD syndrome CHIME syndrome Cardiofaciocutaneous syndrome Cartilage-hair hypoplasia Cataract-hypertrichosis-intellectual disability syndrome Centripetalis recessive dystrophic epidermolysis bullosa Cerebellar ataxia-ectodermal dysplasia syndrome Cervical hypertrichosis-peripheral neuropathy syndrome Chondroectodermal dysplasia with night blindness Choroidal atrophy-alopecia syndrome Cleft lip/palate-ectodermal dysplasia syndrome Cleft lip/palate-ectodermal dysplasia syndrome Conductive deafness-ptosis-skeletal anomalies syndrome Congenital cataract-ichthyosis syndrome Congenital generalized hypertrichosis, Ambras type Congenital ichthyosiform erythroderma Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Congenital ichthyosis-microcephalus-tetraplegia syndrome Congenital reticular ichthyosiform erythroderma Contractures-ectodermal dysplasia-cleft lip/palate syndrome Cooks syndrome Corneodermatoosseous syndrome Crandall syndrome Cranioectodermal dysplasia Cronkhite-Canada syndrome Curly hair-acral keratoderma-caries syndrome DOORS syndrome Dahlberg-Borer-Newcomer syndrome Deafness-enamel hypoplasia-nail defects syndrome Deafness-onychodystrophy syndrome Dermatoosteolysis, Kirghizian type Dermatopathia pigmentosa reticularis Dermoodontodysplasia Dermotrichic syndrome Dubowitz syndrome Dyskeratosis congenita Dystrophic epidermolysis bullosa Dystrophic epidermolysis bullosa pruriginosa EEC syndrome EEC syndrome and related disorders EEM syndrome Ectodermal dysplasia syndrome Ectodermal dysplasia with natal teeth, Turnpenny type Ectodermal dysplasia, trichoodontoonychial type Ectodermal dysplasia-blindness syndrome Ectodermal dysplasia-hyperhidrosis-cutaneous syndactyly syndrome Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome Ectodermal dysplasia-pili torti-cutaneous syndactyly syndrome Ectodermal dysplasia-sensorineural deafness syndrome Ectodermal dysplasia-skin fragility syndrome Ellis Van Creveld syndrome Epidermolysis bullosa simplex Epidermolysis bullosa simplex due to BP230 deficiency Epidermolysis bullosa simplex due to exophilin 5 deficiency Epidermolysis bullosa simplex superficialis Epidermolysis bullosa simplex with anodontia/hypodontia Epidermolysis bullosa simplex with circinate migratory erythema Epidermolysis bullosa simplex with mottled pigmentation Epidermolysis bullosa simplex with muscular dystrophy Epidermolysis bullosa simplex with pyloric atresia Erythrokeratodermia variabilis Exfoliative ichthyosis Familial isolated trichomegaly Focal dermal hypoplasia Focal facial dermal dysplasia Focal facial dermal dysplasia type I Focal facial dermal dysplasia type II Focal facial dermal dysplasia type III Focal facial dermal dysplasia type IV Fried's tooth and nail syndrome Frontal fibrosing alopecia Frontonasal dysplasia-alopecia-genital anomalies syndrome GAPO syndrome Generalized peeling skin syndrome Genetic hair anomaly Gingival fibromatosis-hypertrichosis syndrome Gorlin-Chaudhry-Moss syndrome Graham Little-Piccardi-Lassueur syndrome Hair defect-photosensitivity-intellectual disability syndrome Hallermann-Streiff syndrome Harlequin ichthyosis Hereditary hypotrichosis with recurrent skin vesicles Hidrotic ectodermal dysplasia Hidrotic ectodermal dysplasia, Christianson-Fourie type Hidrotic ectodermal dysplasia, Halal type Hypertrichosis cubiti Hypertrichosis lanuginosa congenita Hypertrichosis-acromegaloid facial appearance syndrome Hypodontia-dysplasia of nails syndrome Hypohidrotic ectodermal dysplasia Hypohidrotic ectodermal dysplasia with immunodeficiency Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome Hypotrichosis simplex Hypotrichosis simplex of the scalp Hypotrichosis with juvenile macular degeneration Hypotrichosis-deafness syndrome Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome Ichthyosis Ichthyosis follicularis-alopecia-photophobia syndrome Ichthyosis hystrix gravior Ichthyosis hystrix of Curth-Macklin Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Ichthyosis-cheek-eyebrow syndrome Ichthyosis-hypotrichosis syndrome Ichthyosis-oral and digital anomalies syndrome Ichthyosis-prematurity syndrome Incontinentia pigmenti Inherited epidermolysis bullosa Inherited ichthyosis syndromic form Intermediate generalized junctional epidermolysis bullosa Isolated anterior cervical hypertrichosis Isolated hair shaft abnormality Ito hypomelanosis Johanson-Blizzard syndrome Johnson neuroectodermal syndrome Junctional epidermolysis bullosa Junctional epidermolysis bullosa inversa Junctional epidermolysis bullosa with pyloric atresia Junctional epidermolysis bullosa, non-Herlitz type KID syndrome Keratinopathic ichthyosis Keratoderma hereditarium mutilans with ichthyosis Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Kindler epidermolysis bullosa Lacrimoauriculodentodigital syndrome Lamellar ichthyosis Laryngo-onycho-cutaneous syndrome Late-onset junctional epidermolysis bullosa Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Lelis syndrome Lethal acantholytic erosive disorder Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome Lichen planopilaris Limb-mammary syndrome Localized dystrophic epidermolysis bullosa, acral form Localized dystrophic epidermolysis bullosa, nails only Localized dystrophic epidermolysis bullosa, pretibial form Localized epidermolysis bullosa simplex Localized junctional epidermolysis bullosa Loose anagen syndrome MEDNIK syndrome Marie Unna hereditary hypotrichosis Marshall syndrome Monilethrix Naegeli-Franceschetti-Jadassohn syndrome Netherton syndrome Noonan syndrome-like disorder with loose anagen hair Oculodentodigital dysplasia Oculoosteocutaneous syndrome Oculotrichodysplasia Odonto-onycho dysplasia-alopecia syndrome Odonto-onycho-dermal dysplasia Odonto-tricho-ungual-digito-palmar syndrome Odontotrichomelic syndrome Orofaciodigital syndrome type 1 Osteosclerosis-ichthyosis-premature ovarian failure syndrome PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement Papillon-Lefèvre syndrome Peeling skin syndrome Peeling skin syndrome type A Peeling skin syndrome type B Peeling skin syndrome type C Pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome Pili bifurcati Pili gemini Pili torti Pili torti-developmental delay-neurological abnormalities syndrome Pili torti-onychodysplasia syndrome Pilodental dysplasia-refractive errors syndrome Pseudopelade of Brocq Pure hair and nail ectodermal dysplasia Pyramidal molars-abnormal upper lip syndrome Quinquaud folliculitis decalvans Rare disorder with hypertrichosis Recessive X-linked ichthyosis Recessive dystrophic epidermolysis bullosa inversa Ringed hair disease Scalp-ear-nipple syndrome Schinzel-Giedion syndrome Schöpf-Schulz-Passarge syndrome Self-improving collodion baby Self-improving dystrophic epidermolysis bullosa Severe generalized junctional epidermolysis bullosa Sjögren-Larsson syndrome Sparse hair-short stature-skin anomalies syndrome Superficial epidermolytic ichthyosis Suprabasal epidermolysis bullosa simplex Syndromic hair shaft abnormality Syndromic recessive X-linked ichthyosis Taurodontia-absent teeth-sparse hair syndrome Teebi-Shaltout syndrome Toriello-Lacassie-Droste syndrome Tricho-dento-osseous syndrome Tricho-oculo-dermo-vertebral syndrome Tricho-retino-dento-digital syndrome Trichodental syndrome Trichodermodysplasia-dental alterations syndrome Trichodysplasia-amelogenesis imperfecta syndrome Trichodysplasia-xeroderma syndrome Trichomegaly-retina pigmentary degeneration-dwarfism syndrome Trichoodontoonychial dysplasia Trichorhinophalangeal syndrome Trichorhinophalangeal syndrome type 1 Trichorhinophalangeal syndrome type 2 Trichothiodystrophy Uncombable hair syndrome Woolly hair Woolly hair nevus Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome X-linked congenital generalized hypertrichosis X-linked dominant chondrodysplasia punctata X-linked hypohidrotic ectodermal dysplasia