SE-ATLAS

Acral peeling skin syndrome Acral self-healing collodion baby Annular epidermolytic ichthyosis 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 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 Basal epidermolysis bullosa simplex Bathing suit ichthyosis CEDNIK syndrome CHILD syndrome Centripetalis recessive dystrophic epidermolysis bullosa Congenital cataract-ichthyosis syndrome Congenital generalized lipodystrophy Congenital ichthyosiform erythroderma Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Congenital ichthyosis-microcephalus-tetraplegia syndrome Congenital reticular ichthyosiform erythroderma Cutaneous mastocytosis Difference of sex development Dystrophic epidermolysis bullosa Dystrophic epidermolysis bullosa pruriginosa Ectodermal dysplasia-skin fragility syndrome Epidermolysis bullosa simplex 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 Epidermolytic nevus Erythrokeratodermia variabilis Exfoliative ichthyosis Familial hyperinsulinism Generalized peeling skin syndrome Harlequin ichthyosis 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-oral and digital anomalies syndrome Ichthyosis-prematurity syndrome Inherited epidermolysis bullosa Inherited ichthyosis syndromic form Intermediate generalized junctional epidermolysis bullosa 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 Lamellar ichthyosis Large congenital melanocytic nevus Laryngo-onycho-cutaneous syndrome Late-onset junctional epidermolysis bullosa Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Leprechaunism Lethal acantholytic erosive disorder 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 MEDNIK syndrome MODY Mastocytosis Neonatal diabetes mellitus Neonatal ichthyosis-sclerosing cholangitis syndrome Netherton syndrome Neurocutaneous melanocytosis Osteosclerosis-ichthyosis-premature ovarian failure syndrome PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement Peeling skin syndrome Peeling skin syndrome type A Peeling skin syndrome type B Peeling skin syndrome type C Rare endocrine disease Rare endocrine growth disease Rare precocious puberty Recessive X-linked ichthyosis Recessive dystrophic epidermolysis bullosa inversa Self-improving collodion baby Self-improving dystrophic epidermolysis bullosa Severe generalized junctional epidermolysis bullosa Sjögren-Larsson syndrome Superficial epidermolytic ichthyosis Suprabasal epidermolysis bullosa simplex Syndromic recessive X-linked ichthyosis Thiamine-responsive megaloblastic anemia syndrome Trichothiodystrophy Wolcott-Rallison syndrome Wolfram syndrome X-linked dominant chondrodysplasia punctata