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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"
Ichthyosis hystrix gravior
Ichthyosis, Lambert type
Autosomal dominant epidermolytic ichthyosis
BCIE · Bullous congenital ichthyosiform erythroderma
Harlequin ichthyosis
HI · Ichthyosis congenita, Harlequin type
Ichthyosis
Ichthyosis-prematurity syndrome
Congenital ichthyosis type 4 · IPS
KID syndrome
KID/HID syndrome · Keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome
Lamellar ichthyosis
LI
Recessive X-linked ichthyosis
RXLI · Steroid sulfatase deficiency