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"

200 matching diseasesClear search ×

BRESEK syndrome

BRESHECK syndrome

ORPHA:85284

21q deletion syndrome

21q- syndrome · Partial 21q monosomy

ORPHA:574

3C syndrome

Craniocerebellocardiac dysplasia · Ritscher-Schinzel syndrome

ORPHA:7

3M syndrome

3-M syndrome · Yakut short stature syndrome

ORPHA:2616

3MC syndrome

Malpuech-Michels-Mingarelli-Carnevale syndrome · Craniofacial-ulnar-renal syndrome

ORPHA:293843

46,XY complete gonadal dysgenesis

46,XY CGD · 46,XY pure gonadal dysgenesis

ORPHA:242

47,XYY syndrome

Jacobs syndrome · Double Y syndrome

ORPHA:8

Absence of fingerprints-congenital milia syndrome

Absence of dermatoglyphics-congenital milia syndrome · Baird syndrome

ORPHA:1658

Acropectorovertebral dysplasia

F syndrome

ORPHA:957

Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome

AMME complex · AMME syndrome

ORPHA:86818

ANE syndrome

Alopecia-progressive neurological defect-endocrinopathy syndrome

ORPHA:157954

Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome

AEC syndrome · Hay-Wells syndrome

ORPHA:1071

Antisynthetase syndrome

AS syndrome · Anti-Jo1 syndrome

ORPHA:81

Aplastic anemia-intellectual disability-dwarfism syndrome

AMeD syndrome

ORPHA:611216

Apparent mineralocorticoid excess

11-beta-hydroxysteroid dehydrogenase deficiency type 2 · Ulick syndrome

ORPHA:320

Arthrogryposis-renal dysfunction-cholestasis syndrome

ARC syndrome

ORPHA:2697

Autoimmune polyendocrinopathy type 1

APECED syndrome · APS type 1

ORPHA:3453

Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency

AD-HIES due to STAT3 deficiency · Autosomal dominant HIES due to STAT3 deficiency

ORPHA:2314

B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome

BILU syndrome · Hoffman syndrome

ORPHA:567502

Balint syndrome

Balint-Holmes syndrome · Optic ataxia-gaze apraxia-simultanagnosia syndrome

ORPHA:363746

Ballard syndrome

Pitt-Williams brachydactyly · Brachydactyly, combined B and E types

ORPHA:93395

Banki syndrome

ORPHA:1228

Barth syndrome

3-methylglutaconic aciduria type 2 · BTHS

ORPHA:111

Bartter syndrome

Renal tubular normotensive hypokalemic alkalosis with hypercalciuria · Salt-losing tubular disorder, Henle's loop type

ORPHA:112

Bazex syndrome

Acrokeratosis of Bazex · Acrokeratosis paraneoplastica

ORPHA:166113

Behr syndrome

Behr complicated familial optic atrophy

ORPHA:1239

Bencze syndrome

Hemifacial hyperplasia-strabismus syndrome

ORPHA:1241

BIDS syndrome

Amish brittle hair syndrome · Trichothiodystrophy type D

ORPHA:1245

Biliary atresia with splenic malformation syndrome

BASM syndrome

ORPHA:244283

Blau syndrome

ORPHA:90340

Blepharo-cheilo-odontic syndrome

BCD syndrome · Blepharocheilodontic syndrome

ORPHA:1997

Blepharophimosis-intellectual disability syndrome, Ohdo type

BMRS, Ohdo type · Blepharophimosis syndrome, Ohdo type

ORPHA:2728

Bloom syndrome

BSyn

ORPHA:125

Blue rubber bleb nevus

Bean syndrome · BRBN

ORPHA:1059

BNAR syndrome

Bifid nose with or without anorectal and renal anomalies

ORPHA:217266

Bohring-Opitz syndrome

BOS syndrome · Bohring syndrome

ORPHA:97297

Böök syndrome

ORPHA:1262

BOR syndrome

Branchiootorenal syndrome · Branchiootorenal spectrum disorder

ORPHA:107

Bowen syndrome

ORPHA:1271

Brachydactyly-nystagmus-cerebellar ataxia syndrome

Biemond syndrome

ORPHA:1246

Brachymorphism-onychodysplasia-dysphalangism syndrome

BOD syndrome · Senior syndrome

ORPHA:1292

Braddock syndrome

Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency

ORPHA:52047

Braddock-Carey syndrome

Thrombocytopenia-Robin sequence syndrome

ORPHA:3323

Branchioskeletogenital syndrome

Elsahy-Waters syndrome · BSG syndrome

ORPHA:1299

Bruck syndrome

Osteogenesis imperfecta-congenital joint contractures syndrome

ORPHA:2771

Brugada syndrome

Ventricular fibrillation, Brugada type

ORPHA:130

C syndrome

OTCS · Opitz C trigonocephaly

ORPHA:1308

CACH syndrome

Childhood ataxia with diffuse central nervous system hypomyelination · Leukoencephalopathy with vanishing white matter

ORPHA:135