Rare Disease Library

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"

20 matching diseasesClear search ×

X-linked ichthyosis syndrome

ORPHA:281210

Recessive X-linked ichthyosis

RXLI · Steroid sulfatase deficiency

ORPHA:461

Syndromic recessive X-linked ichthyosis

Syndromic RXLI · Recessive X-linked ichthyosis with extracutaneous manifestations

ORPHA:281090

Acquired ichthyosis

ORPHA:454

Autosomal dominant epidermolytic ichthyosis

BCIE · Bullous congenital ichthyosiform erythroderma

ORPHA:312

Congenital reticular ichthyosiform erythroderma

CRIE · IWC

ORPHA:281190

Harlequin ichthyosis

HI · Ichthyosis congenita, Harlequin type

ORPHA:457

Hydrocephalus with stenosis of the aqueduct of Sylvius

Bickers-Adams syndrome · HSAS

ORPHA:2182

Ichthyosis

ORPHA:79354

Ichthyosis hystrix gravior

Ichthyosis, Lambert type

ORPHA:79504

Inherited ichthyosis

Genetic ichthyosis

ORPHA:183435

Isolated growth hormone deficiency type III

Congenital IGHD type III · Congenital isolated GH deficiency type III

ORPHA:231692

Kennedy disease

SBMA · X-linked BSMA

ORPHA:481

Lamellar ichthyosis

LI

ORPHA:313

X-linked adrenal hypoplasia congenita

X-linked congenital adrenal hypoplasia · X-linked AHC

ORPHA:95702

X-linked adrenoleukodystrophy

ALD · X-ALD

ORPHA:43

X-linked distal hereditary motor neuropathy

X-linked dHMN · X-linked distal spinal muscular atrophy

ORPHA:404538

X-linked Ehlers-Danlos syndrome

EDS V · Ehlers-Danlos syndrome type 5

ORPHA:75497

X-linked mendelian susceptibility to mycobacterial diseases

X-linked MSMD

ORPHA:319605

X-linked scapuloperoneal muscular dystrophy

X-linked SPMD · X-linked scapuloperoneal syndrome

ORPHA:431272