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Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.
Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"
Congenital ichthyosiform erythroderma
CIE · Erythrodermic ichthyosis
Autosomal dominant epidermolytic ichthyosis
BCIE · Bullous congenital ichthyosiform erythroderma
CHILD syndrome
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects · CHILD nevus
Congenital lethal erythroderma
Congenital reticular ichthyosiform erythroderma
CRIE · IWC
Kindler epidermolysis bullosa
Kindler syndrome · Poikiloderma of Kindler