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 ×

Bohring-Opitz syndrome

BOS syndrome · Bohring syndrome

ORPHA:97297

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

47,XYY syndrome

Jacobs syndrome · Double Y syndrome

ORPHA:8

Abruzzo-Erickson syndrome

CHARGE-like syndrome · Cleft palate-coloboma-deafness syndrome

ORPHA:921

Acrocardiofacial syndrome

ACFS · CCGE syndrome

ORPHA:2008

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

Arthrogryposis-renal dysfunction-cholestasis syndrome

ARC syndrome

ORPHA:2697

Autoimmune interstitial lung disease-arthritis syndrome

COPA syndrome

ORPHA:444092

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

Autosomal recessive faciodigitogenital syndrome

Aarskog-like syndrome · Facio-digito-genital syndrome, Kuwait type

ORPHA:1974

Autosomal recessive spastic paraplegia type 23

Lison syndrome · SPG23

ORPHA:101003

Blepharo-cheilo-odontic syndrome

BCD syndrome · Blepharocheilodontic syndrome

ORPHA:1997

Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency

PXE-like syndrome · Pseudoxanthoma elasticum-like syndrome

ORPHA:91135

BOR syndrome

Branchiootorenal syndrome · Branchiootorenal spectrum disorder

ORPHA:107

Brachydactyly-elbow wrist dysplasia syndrome

Brachydactyly-joint dysplasia syndrome · Liebenberg syndrome

ORPHA:1275

Brachymorphism-onychodysplasia-dysphalangism syndrome

BOD syndrome · Senior syndrome

ORPHA:1292

Branchioskeletogenital syndrome

Elsahy-Waters syndrome · BSG syndrome

ORPHA:1299

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

CAMFAK syndrome

CAMAK syndrome · Cataract-microcephaly-arthrogryposis-kyphosis syndrome

ORPHA:1317

CAMOS syndrome

Cerebellar ataxia-intellectual disability-optic atrophy-skin abnormalities syndrome · SCAR5

ORPHA:83472

Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome

Pericarditis-arthropathy-camptodactyly syndrome · Arthropathy-camptodactyly syndrome

ORPHA:2848

Camptodactyly-tall stature-scoliosis-hearing loss syndrome

Camptodactyly-tall stature-scoliosis-deafness syndrome · CATSHL syndrome

ORPHA:85164

Cancer-associated retinopathy

CAR syndrome · Paraneoplastic retinopathy

ORPHA:71505

CANDLE syndrome

Chronic atypical neutrophilic dermatosis-lipodystrophy-elevated temperature syndrome

ORPHA:325004

CANOMAD syndrome

Chronic ataxic neuropathy-ophthalmoplegia-IgM paraprotein-cold agglutinins-disialosyl antibodies syndrome · Chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies

ORPHA:71279

Cantú syndrome

Hypertrichotic osteochondrodysplasia · Congenital hypertrichosis-coarse facial features spectrum

ORPHA:1517

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

Carney complex

Carney syndrome · Myxoma-spotty pigmentation-endocrine overactivity syndrome

ORPHA:1359

Caroli syndrome

ORPHA:480520

Cataract-hypertrichosis-intellectual disability syndrome

CAHMR syndrome

ORPHA:1375

Cataract-nephropathy-encephalopathy syndrome

Crome syndrome

ORPHA:1380

CEDNIK syndrome

Cerebral dysgenesis-neuropathy-ichthyosis-palmoplantar keratoderma syndrome

ORPHA:66631

Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

CANVAS · Cerebellar ataxia with bilateral vestibulopathy syndrome

ORPHA:504476

Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome

Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural deafness syndrome · CAPOS syndrome

ORPHA:1171

Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome

CIMDAG syndrome

ORPHA:603448

CHAND syndrome

Baughman syndrome · CHANDS

ORPHA:1401

Char syndrome

Patent ductus arteriosus with facial dysmorphism and abnormal fifth digits

ORPHA:46627