SE-ATLAS

Autosomal dominant primary microcephaly KID syndrome CEDNIK syndrome Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion Congenital reticular ichthyosiform erythroderma Ichthyosis-cheek-eyebrow syndrome Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Netherton syndrome Congenital ichthyosis-microcephalus-tetraplegia syndrome Ichthyosis-oral and digital anomalies syndrome Neurofibromatosis type 1 Ichthyosis follicularis-alopecia-photophobia syndrome Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Isolated congenital microcephaly Ichthyosis-prematurity syndrome Ichthyosis Syndromic recessive X-linked ichthyosis X-linked dominant chondrodysplasia punctata Ichthyosis hystrix of Curth-Macklin Inherited ichthyosis syndromic form Autosomal ichthyosis syndrome with prominent hair abnormalities Ichthyosis hystrix gravior Huntington disease Autosomal recessive congenital ichthyosis Sjögren-Larsson syndrome Autosomal ichthyosis syndrome with fatal disease course Peeling skin syndrome MEDNIK syndrome Autosomal ichthyosis syndrome with other associated signs CHILD syndrome Autosomal ichthyosis syndrome with prominent neurologic signs Campomelic dysplasia Keratinopathic ichthyosis Congenital cataract-ichthyosis syndrome Congenital ichthyosiform erythroderma Rare genetic skin disease Self-improving collodion baby Keratoderma hereditarium mutilans with ichthyosis Ichthyosis-hypotrichosis syndrome Acral peeling skin syndrome 17q11 microdeletion syndrome Acral self-healing collodion baby Exfoliative ichthyosis Annular epidermolytic ichthyosis Generalized peeling skin syndrome Peeling skin syndrome type A Osteosclerosis-ichthyosis-premature ovarian failure syndrome Autosomal dominant epidermolytic ichthyosis Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Lamellar ichthyosis Erythrokeratodermia variabilis Bathing-suit-Ichthyose Ichthyose, epidermolytische superfizielle Harlekin-Ichthyose Peeling-Skin-Syndrom Typ B Lissenzephalie Ichthyose, X-chromosomal-rezessive Peeling-Skin-Syndrom, generalisiertes, Typ C Mikrozephalie, primäre, autosomal-rezessive