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"

138 matching diseasesClear search ×

Heart-hand syndrome type 3

Atriodigital dysplasia type 3 · Cardiomelic syndrome type 3

ORPHA:1342

22q11.2 deletion syndrome

22q11DS · CATCH 22

ORPHA:567

3M syndrome

3-M syndrome · Yakut short stature syndrome

ORPHA:2616

Aase-Smith syndrome type 1

Aase-Smith I syndrome · Hydrocephalus-cleft palate-joint contractures syndrome

ORPHA:916

Aicardi syndrome

Agenesis of corpus callosum with chorioretinal abnormality

ORPHA:50

ALG1-CDG

CDG syndrome type Ik · CDG-Ik

ORPHA:79327

ALG11-CDG

CDG syndrome type Ip · CDG-Ip

ORPHA:280071

ALG12-CDG

CDG syndrome type Ig · CDG-Ig

ORPHA:79324

ALG13-CDG

Congenital disorder of glycosylation type Is · CDG syndrome type Is

ORPHA:324422

ALG2-CDG

CDG syndrome type Ii · CDG-Ii

ORPHA:79326

ALG3-CDG

CDG syndrome type Id · CDG-Id

ORPHA:79321

ALG6-CDG

CDG syndrome type Ic · CDG-Ic

ORPHA:79320

ALG8-CDG

CDG syndrome type Ih · CDG-Ih

ORPHA:79325

ALG9-CDG

CDG syndrome type IL · CDG1L

ORPHA:79328

Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16

ATR syndrome linked to chromosome 16 · ATR syndrome, deletion type

ORPHA:98791

Andersen-Tawil syndrome

Andersen syndrome · LQT7

ORPHA:37553

Autosomal dominant otospondylomegaepiphyseal dysplasia

AD OSMED · Stickler syndrome type 3

ORPHA:166100

B4GALT1-CDG

Beta-1,4-galactosyltransferase deficiency · CDG syndrome type IId

ORPHA:79332

Bartter syndrome type 1

Bartter syndrome type I

ORPHA:620217

Bartter syndrome type 2

Bartter syndrome type II

ORPHA:620220

Bartter syndrome type 3

Bartter syndrome type III

ORPHA:93605

Bartter syndrome type 4

Bartter syndrome with sensorineural hearing loss · Bartter syndrome with sensorineural deafness

ORPHA:89938

Biemond syndrome type 2

Hypogonadism-short stature-coloboma-preaxial polydactyly syndrome

ORPHA:141333

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

CAD-CDG

CDG-Iz · Congenital disorder of glycosylation type 1z

ORPHA:448010

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 syndrome, Guadalajara type 3

ORPHA:488434

Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome

Pericarditis-arthropathy-camptodactyly syndrome · Arthropathy-camptodactyly syndrome

ORPHA:2848

Cancer-associated retinopathy

CAR syndrome · Paraneoplastic retinopathy

ORPHA:71505

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

Carcinoid syndrome

Malignant carcinoid syndrome

ORPHA:100093

Cardiocranial syndrome, Pfeiffer type

Craniosynostosis-congenital heart disease-intellectual disability syndrome · Pfeiffer-Singer-Zschiesche syndrome

ORPHA:2872

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

Carpenter syndrome

ACPS2 · Acrocephalopolysyndactyly type 2

ORPHA:65759

Carvajal syndrome

Wooly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome · Wooly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome

ORPHA:65282

Cataract-hypertrichosis-intellectual disability syndrome

CAHMR syndrome

ORPHA:1375

CCDC115-CDG

CDG syndrome type IIo · CDG-IIo

ORPHA:468684

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

Chronic atrial and intestinal dysrhythmia syndrome

CAID syndrome · Chronic atrial dysrhythmia-intestinal motility disorder

ORPHA:435988

Chronic Epstein-Barr virus infection syndrome

Chronic EBV infection syndrome · CAEBV syndrome

ORPHA:2566

Cleidorhizomelic syndrome

Rhizomelic shortness with clavicular defect · Wallis-Zieff-Goldblatt syndrome

ORPHA:1453