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 ×

Branchioskeletogenital syndrome

Elsahy-Waters syndrome · BSG syndrome

ORPHA:1299

BRESEK syndrome

BRESHECK syndrome

ORPHA:85284

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

Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome

Pericarditis-arthropathy-camptodactyly syndrome · Arthropathy-camptodactyly syndrome

ORPHA:2848

Cancer-associated retinopathy

CAR syndrome · Paraneoplastic retinopathy

ORPHA:71505

Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome

PHD syndrome · Polyvalvular heart disease syndrome

ORPHA:228410

Cardiofaciocutaneous syndrome

CFC syndrome

ORPHA:1340

Carnevale syndrome

3MC2 syndrome · Carnevale-Krajewska-Fischetto syndrome

ORPHA:2998

Cataract-nephropathy-encephalopathy syndrome

Crome syndrome

ORPHA:1380

Childhood disintegrative disorder

Heller syndrome · Dementia infantilis

ORPHA:168782

Chronic intestinal pseudoobstruction syndrome

CIPO · CIP syndrome

ORPHA:2978

CK syndrome

X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome

ORPHA:251383

CNTNAP2-related developmental and epileptic encephalopathy

CDFE syndrome · CDFES

ORPHA:163681

Congenital contractural arachnodactyly

Beals syndrome · Beals-Hecht syndrome

ORPHA:115

Congenital generalized hypertrichosis, Ambras type

Ambras syndrome

ORPHA:1023

Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome

Bassoe syndrome

ORPHA:1875

Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome

SIFD syndrome

ORPHA:369861

Corneodermatoosseous syndrome

CDO syndrome · Stern-Lubinsky-Durrie syndrome

ORPHA:3194

Costello syndrome

FCS syndrome · Faciocutaneoskeletal syndrome

ORPHA:3071

CPE-related Prader-Willi-like syndrome

BDV syndrome · Blakemore-Durmaz-Vasileiou syndrome

ORPHA:633028

Craniosynostosis-anal anomalies-porokeratosis syndrome

CAP syndrome · CDAGS syndrome

ORPHA:85199

Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome

Berant syndrome · Capra-DeMarco syndrome

ORPHA:171839

Deafness-enamel hypoplasia-nail defects syndrome

Heimler syndrome · Hearing loss-enamel hypoplasia-nail defects syndrome

ORPHA:3220

Diethylstilbestrol syndrome

DES embryofetopathy · DES syndrome

ORPHA:1916

Digitorenocerebral syndrome

DRC syndrome · Eronen-Somer-Gustafsson syndrome

ORPHA:1674

Distal deletion 3p syndrome

3p- syndrome · Distal monosomy 3p

ORPHA:1620

Double uterus-hemivagina-renal agenesis syndrome

Double uterus and obstructed hemivagina syndrome · OHVIRA syndrome

ORPHA:3411

Down syndrome

Trisomy 21

ORPHA:870

Ectrodactyly-cleft palate syndrome

ECP syndrome

ORPHA:1889

EEC syndrome

Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome

ORPHA:1896

EEM syndrome

Ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome

ORPHA:1897

Endocrine-cerebro-osteodysplasia syndrome

ECO syndrome

ORPHA:199332

Erythrokeratodermia-cardiomyopathy syndrome

EKC syndrome

ORPHA:476096

Feingold syndrome

Brunner-Winter syndrome · Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum

ORPHA:1305

Fowler urethral sphincter dysfunction syndrome

Fowler-Christmas-Chapple syndrome · Fowler syndrome

ORPHA:2795

Fraser syndrome

Cryptophthalmos-syndactyly syndrome

ORPHA:2052

Frasier syndrome

ORPHA:347

Frey syndrome

Baillarger syndrome · Auriculotemporal syndrome

ORPHA:662240

Gardner syndrome

ORPHA:79665

GMS syndrome

Goniodysgenesis-intellectual disability-short stature syndrome

ORPHA:2090

Gorlin-Chaudhry-Moss syndrome

Craniofacial dysostosis-genital, dental, cardiac anomalies syndrome · Cranofacial dysostosis-hypertrichosis-hypoplasia of labia majora syndrome

ORPHA:2095

H syndrome

ORPHA:168569

HEC syndrome

Hydrocephalus-endocardial fibroelastosis-cataract syndrome

ORPHA:2119

Heiner syndrome

Cow's milk-induced pulmonary hypersensitivity syndrome

ORPHA:99932

Hemiconvulsion-hemiplegia-epilepsy syndrome

HHE · HHE syndrome

ORPHA:86908

Holmes-Adie syndrome

Tonic pupil-tendon areflexia syndrome · Adie syndrome

ORPHA:454718