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"

21 matching diseasesClear search ×

OBSOLETE: Congenital liver hemangioma

OBSOLETE: Congenital hepatic hemangioma

ORPHA:238691

Congenital anomaly of hepatic vein

ORPHA:95507

Congenital hemangioma

ORPHA:458775

Isolated congenital hepatic fibrosis

Isolated CHF

ORPHA:485426

Non-involuting congenital hemangioma

NICH

ORPHA:141179

OBSOLETE: Acheiria, bilateral

OBSOLETE: Congenital absence of hand, bilateral

ORPHA:295103

OBSOLETE: Adactyly of foot

OBSOLETE: Congenital absence of toes

ORPHA:435623

OBSOLETE: Congenital aortic valve insufficiency

ORPHA:95449

OBSOLETE: Congenital cataract, Volkmann type

ORPHA:98983

OBSOLETE: Congenital entropion

ORPHA:98568

OBSOLETE: Congenital hydromyelia

ORPHA:268874

OBSOLETE: Congenital hydronephrosis

ORPHA:2190

OBSOLETE: Congenital myopathy with vacuoles

ORPHA:172985

OBSOLETE: Congenital neuronal ceroid lipofuscinosis

OBSOLETE: Congenital NCL

ORPHA:168486

OBSOLETE: Congenital valvular dysplasia

ORPHA:1864

OBSOLETE: Conjunctival hemangioma or hemolymphangioma

ORPHA:98612

OBSOLETE: Familial capillary hemangioma

ORPHA:91415

OBSOLETE: Giant infantile hemangioma

ORPHA:210592

OBSOLETE: Terminal transverse defects of arm

OBSOLETE: Congenital limb amputation

ORPHA:93937

Partially involuting congenital hemangioma

ORPHA:458785

Rapidly involuting congenital hemangioma

RICH

ORPHA:141184