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 ×

Dysbetalipoproteinemia

Remnant hyperlipoproteinemia · HLP type 3

ORPHA:412

Autoimmune polyendocrinopathy type 3

APS type 3 · APS3

ORPHA:227982

Congenital dyserythropoietic anemia type III

CDA III · CDA type 3

ORPHA:98870

Congenital pulmonary airway malformation type 3

CCAM type 3 · CPAM type 3

ORPHA:280847

Familial hypocalciuric hypercalcemia type 3

FHH type 3

ORPHA:101050

Glycogen storage disease due to glycogen debranching enzyme deficiency

GSDIII · Glycogen storage disease type 3

ORPHA:366

Hyperlipoproteinemia type 1

HLP type 1

ORPHA:411

Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome

MCAHS type 3 · Multiple congenital anomalies-hypotonia-seizures syndrome type 3

ORPHA:369837

Midline interhemispheric variant of holoprosencephaly

MIH · MIH type HPE

ORPHA:93926

OBSOLETE: Hyperlipoproteinemia type 5

OBSOLETE: HLP type 5 · OBSOLETE: Major hyperlipidemia

ORPHA:70470

Osteogenesis imperfecta type 3

OI type 3 · Progressive deforming osteogenesis imperfecta

ORPHA:216812

Progressive myoclonic epilepsy type 3

EPM3 · PME type 3

ORPHA:263516

Proximal spinal muscular atrophy type 3

Juvenile spinal muscular atrophy · Kugelberg-Welander disease

ORPHA:83419