SE-ATLAS

Congenital cataract-ichthyosis syndrome Keratoderma hereditarium mutilans with ichthyosis Congenital ichthyosiform erythroderma Epidermolysis bullosa simplex with mottled pigmentation Autosomal dominant generalized epidermolysis bullosa simplex, severe form Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form Localized junctional epidermolysis bullosa PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement Localized epidermolysis bullosa simplex Junctional epidermolysis bullosa with pyloric atresia Intermediate generalized junctional epidermolysis bullosa Self-improving collodion baby Junctional epidermolysis bullosa inversa Severe generalized junctional epidermolysis bullosa Late-onset junctional epidermolysis bullosa Acral self-healing collodion baby Localized dystrophic epidermolysis bullosa, pretibial form Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form Dystrophic epidermolysis bullosa Recessive dystrophic epidermolysis bullosa inversa Wolcott-Rallison syndrome Acral peeling skin syndrome Epidermolysis bullosa simplex Self-improving dystrophic epidermolysis bullosa Exfoliative ichthyosis Junctional epidermolysis bullosa Peeling skin syndrome type A Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Osteosclerosis-ichthyosis-premature ovarian failure syndrome Autosomal dominant epidermolytic ichthyosis Generalized peeling skin syndrome Annular epidermolytic ichthyosis Lamellar ichthyosis Suprabasal epidermolysis bullosa simplex Ectodermal dysplasia-skin fragility syndrome Erythrokeratodermia variabilis Basal epidermolysis bullosa simplex Kindler epidermolysis bullosa Epidermolytic nevus Thiamine-responsive megaloblastic anemia syndrome Bathing suit ichthyosis Superficial epidermolytic ichthyosis Rare endocrine disease Harlequin ichthyosis Peeling skin syndrome type B Localized dystrophic epidermolysis bullosa, nails only Recessive X-linked ichthyosis Wolfram syndrome Localized dystrophic epidermolysis bullosa, acral form Peeling skin syndrome type C Epidermolysis bullosa simplex with circinate migratory erythema Epidermolysis bullosa simplex with pyloric atresia Familial hyperinsulinism Lethal acantholytic erosive disorder KID syndrome Difference of sex development CEDNIK syndrome Trichothiodystrophy Ichthyosis-cheek-eyebrow syndrome Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Neonatal diabetes mellitus Laryngo-onycho-cutaneous syndrome Netherton syndrome Congenital ichthyosis-microcephalus-tetraplegia syndrome Ichthyosis-oral and digital anomalies syndrome Ichthyosis follicularis-alopecia-photophobia syndrome Congenital reticular ichthyosiform erythroderma Epidermolysis bullosa simplex superficialis Autosomal recessive generalized epidermolysis bullosa simplex Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Centripetalis recessive dystrophic epidermolysis bullosa Junctional epidermolysis bullosa, non-Herlitz type Rare precocious puberty Dystrophic epidermolysis bullosa pruriginosa Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form Leprechaunism Ichthyosis-prematurity syndrome Neonatal ichthyosis-sclerosing cholangitis syndrome Ichthyosis Autosomal dominant generalized dystrophic epidermolysis bullosa Inherited epidermolysis bullosa Congenital generalized lipodystrophy Syndromic recessive X-linked ichthyosis X-linked dominant chondrodysplasia punctata Epidermolysis bullosa simplex with muscular dystrophy Ichthyosis hystrix of Curth-Macklin Autosomal ichthyosis syndrome with prominent hair abnormalities Inherited ichthyosis syndromic form Ichthyosis hystrix gravior Autosomal recessive congenital ichthyosis Rare endocrine growth disease MEDNIK syndrome Sjögren-Larsson syndrome Peeling skin syndrome Autosomal ichthyosis syndrome with other associated signs CHILD syndrome Autosomal ichthyosis syndrome with prominent neurologic signs Keratinopathic ichthyosis Epidermolysis bullosa simplex with anodontia/hypodontia MODY Autosomal ichthyosis syndrome with fatal disease course Large congenital melanocytic nevus Neurocutaneous melanocytosis Cutaneous mastocytosis Mastocytosis