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"

13 matching diseasesClear search ×

Acquired pseudoxanthoma elasticum

Acquired Gronblad-Strandberg-Touraine syndrome · Acquired PXE

ORPHA:228247

Acquired angioedema

AAE · Acquired C1 inhibitor deficiency

ORPHA:91385

Acquired arginine vasopressin deficiency

Acquired CDI · Acquired neurogenic diabetes insipidus

ORPHA:95626

Acquired ataxia

ORPHA:247242

Acquired cutis laxa

Cutis laxa acquisita

ORPHA:228285

Acquired hemophilia A

Acquired factor VIII deficiency · Acquired F8 deficiency

ORPHA:599480

Acquired ichthyosis

ORPHA:454

Acquired neutropenia

Immunologic neutropenia

ORPHA:178996

Acquired porencephaly

ORPHA:314697

Alpha-thalassemia-myelodysplastic syndrome

Acquired HbH disease · Acquired hemoglobin H disease

ORPHA:231401

Immune-mediated thrombotic thrombocytopenic purpura

Acquired thrombotic thrombocytopenic purpura · Acquired TTP

ORPHA:93585

Myasthenia gravis

Acquired myasthenia · Autoimmune myasthenia gravis

ORPHA:589

Primary acquired pure red cell aplasia

Primary acquired PRCA

ORPHA:98872