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"

22 matching diseasesClear search ×

Gliomatosis cerebri

ORPHA:251582

Glial tumor

Glioma

ORPHA:182067

Anaplastic ganglioglioma

ORPHA:251957

Anaplastic oligodendroglioma

ORPHA:251630

Angiocentric glioma

ORPHA:251671

Chordoid glioma

ORPHA:251674

Desmoplastic infantile astrocytoma/ganglioglioma

DIA/DIG

ORPHA:251940

Diffuse intrinsic pontine glioma

DIPG

ORPHA:497188

Ganglioglioma

ORPHA:251949

Hereditary pheochromocytoma-paraganglioma

Familial pheochromocytoma-paraganglioma

ORPHA:29072

Infant-type hemispheric glioma

IHG

ORPHA:695136

Multiple paragangliomas associated with polycythemia

Multiple paragangliomas associated with erythrocytosis · Paraganglioma-somatostatinoma-polycythemia syndrome

ORPHA:324299

Nasal ganglioglioma

ORPHA:141115

Non-functioning paraganglioma

Non-secreting paraganglioma

ORPHA:94080

OBSOLETE: Sporadic secreting paraganglioma

ORPHA:276627

Oligodendroglioma

ORPHA:251627

Optic pathway glioma

ORPHA:2086

Osteoporosis-pseudoglioma syndrome

OPPG

ORPHA:2788

Sporadic pheochromocytoma/secreting paraganglioma

ORPHA:276621

Glioblastoma

GBM · Glioblastoma multiforme

ORPHA:360

Gliosarcoma

ORPHA:251576

Nasal glial heterotopia

Nasal glioma

ORPHA:141112