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:
17q11 microdeletion syndrome Acral peeling skin syndrome Acral self-healing collodion baby Annular epidermolytic ichthyosis Autosomal dominant epidermolytic ichthyosis Autosomal dominant primary microcephaly 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 primary microcephaly Bathing suit ichthyosis CEDNIK syndrome CHILD syndrome Campomelic dysplasia Congenital cataract-ichthyosis syndrome Congenital ichthyosiform erythroderma Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Congenital ichthyosis-microcephalus-tetraplegia syndrome Congenital reticular ichthyosiform erythroderma Erythrokeratodermia variabilis Exfoliative ichthyosis Generalized peeling skin syndrome Harlequin ichthyosis Huntington disease 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 Inherited ichthyosis syndromic form Isolated congenital microcephaly KID syndrome Keratinopathic ichthyosis Keratoderma hereditarium mutilans with ichthyosis Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Lamellar ichthyosis Lissencephaly MEDNIK syndrome Netherton syndrome Neurofibromatosis type 1 Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion Osteosclerosis-ichthyosis-premature ovarian failure syndrome Peeling skin syndrome Peeling skin syndrome type A Peeling skin syndrome type B Peeling skin syndrome type C Rare genetic skin disease Recessive X-linked ichthyosis Self-improving collodion baby Sjögren-Larsson syndrome Superficial epidermolytic ichthyosis Syndromic recessive X-linked ichthyosis X-linked dominant chondrodysplasia punctata