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"

12 matching diseasesClear search ×

Atrial septal defect-atrioventricular conduction defects syndrome

ORPHA:1479

Atrial septal defect, coronary sinus type

ASD, coronary sinus type · Unroofed coronary sinus

ORPHA:99104

Atrial septal defect, ostium primum type

ASD, ostium primum type

ORPHA:99106

Atrial septal defect, ostium secundum type

ASD, ostium secundum type

ORPHA:99103

Atrial septal defect, sinus venosus type

ASD, sinus venosus type

ORPHA:99105

Interatrial communication

ASD · Atrial septal defect

ORPHA:1478

Lymphedema-atrial septal defects-facial changes syndrome

Irons-Bianchi syndrome · Irons-Bhan syndrome

ORPHA:86915

Atrial septal aneurysm

ORPHA:99107

Atrioventricular septal defect

AVSD · Atrioventricular canal defect

ORPHA:98722

Complete atrioventricular septal defect

CAVC · Complete atrioventricular canal defect

ORPHA:1329

Partial atrioventricular septal defect

PAVC · Partial atrioventricular canal defect

ORPHA:1330

Pulmonary atresia with ventricular septal defect

ORPHA:1207