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 ×

Neuromyelitis optica spectrum disorder

Devic disease · Devic syndrome

ORPHA:71211

Neuromyelitis optica spectrum disorder with anti-AQP4 antibodies

Devic disease · Devic syndrome

ORPHA:592850

Neuromyelitis optica spectrum disorder with anti-MOG antibodies

Devic disease · Devic syndrome

ORPHA:592856

Neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies

Devic disease · Devic syndrome

ORPHA:592869

21q deletion syndrome

21q- syndrome · Partial 21q monosomy

ORPHA:574

2q13 microdeletion syndrome

del2q13 syndrome

ORPHA:684742

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

3q26 microduplication syndrome

Dup(3)(q26) · Trisomy 3q26

ORPHA:96095

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

5q22 microdeletion syndrome

Monosomy 5q22 syndrome · Del(5)(q22) syndrome

ORPHA:261584

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 polyendocrinopathy type 1

APECED syndrome · APS type 1

ORPHA:3453

Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome

ADCA-DN syndrome · Autosomal dominant cerebellar ataxia-hearing loss-narcolepsy syndrome

ORPHA:314404

Autosomal dominant deafness-onychodystrophy syndrome

DDOD syndrome · Autosomal dominant hearing loss-onychodystrophy syndrome

ORPHA:79499

Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency

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

ORPHA:2314

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

BNAR syndrome

Bifid nose with or without anorectal and renal anomalies

ORPHA:217266

Bohring-Opitz syndrome

BOS syndrome · Bohring syndrome

ORPHA:97297

BOR syndrome

Branchiootorenal syndrome · Branchiootorenal spectrum disorder

ORPHA:107

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

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

Celiac artery compression syndrome

Dunbar syndrome · Median arcuate ligament syndrome

ORPHA:293208

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

SIFD syndrome

ORPHA:369861

Constitutional mismatch repair deficiency syndrome

CMMR-D syndrome

ORPHA:252202

Contractures-webbed neck-micrognathia-hypoplastic nipples syndrome

Dinno syndrome

ORPHA:314002

Corneodermatoosseous syndrome

CDO syndrome · Stern-Lubinsky-Durrie syndrome

ORPHA:3194