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"

15 matching diseasesClear search ×

Complex vascular malformation with associated anomalies

Hemangiolymphangioma

ORPHA:211277

Congenital hemangioma

ORPHA:458775

Diffuse lymphatic malformation

Diffuse lymphangioma · Diffuse lymphangiomatosis

ORPHA:141209

Epithelioid hemangioma

EH · Angiolymphoid hyperplasia with eosinophilia

ORPHA:675396

Genetic complex vascular malformation with associated anomalies

Genetic hemangiolymphangioma

ORPHA:459537

Hemangioblastoma

ORPHA:252054

Hobnail hemangioma

HH · Targetoid hemosiderotic hemangioma

ORPHA:675362

Intravascular papillary endothelial hyperplasia

IPEH · Vegetant intravascular hemangioendothelioma

ORPHA:673525

Isolated rare lymphatic malformation

LM · Lymphangioma

ORPHA:2415

Macrocystic lymphatic malformation

Cavernous lymphangioma · Cavernous lymphatic malformation

ORPHA:79489

Microcystic lymphatic malformation

Capillary lymphangioma · Capillary lymphatic malformation

ORPHA:79490

OBSOLETE: Conjunctival hemangioma or hemolymphangioma

ORPHA:98612

Papillary hemangioma

Papillary capillary hemangioma

ORPHA:673543

Spindle cell hemangioma

Spindle cell hemangioendothelioma

ORPHA:210584

Verrucous hemangioma

ORPHA:464318