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"

117 matching diseasesClear search ×

Cockayne syndrome type 3

Cockayne syndrome type III

ORPHA:90324

Aase-Smith syndrome type 1

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

ORPHA:916

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

Autoimmune interstitial lung disease-arthritis syndrome

COPA syndrome

ORPHA:444092

Autosomal dominant dystrophic epidermolysis bullosa, Cockayne-Touraine type

DDEB, Cockayne-Touraine type

ORPHA:79407

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

CAD-CDG

CDG-Iz · Congenital disorder of glycosylation type 1z

ORPHA:448010

CCDC115-CDG

CDG syndrome type IIo · CDG-IIo

ORPHA:468684

Cocaine embryofetopathy

Fetal cocaine syndrome

ORPHA:1911

Cockayne syndrome

ORPHA:191

Cockayne syndrome type 1

Cockayne syndrome type I

ORPHA:90321

Cockayne syndrome type 2

Cockayne syndrome type II

ORPHA:90322

CODAS syndrome

Cerebrooculodentoauriculoskeletal syndrome

ORPHA:1458

COFS syndrome

Cerebrooculofacioskeletal syndrome · Pena-Shokeir syndrome type 2

ORPHA:1466

COG1-CDG

Congenital disorder of glycosylation type 2g · CDG syndrome type IIg

ORPHA:263508

COG4-CDG

Congenital disorder of glycosylation type 2j · CDG syndrome type IIj

ORPHA:263501

COG5-CDG

CDG syndrome type IIi · CDG-IIi

ORPHA:263487

COG6-CGD

CDG2L · CDG syndrome type IIL

ORPHA:464443

COG7-CDG

CDG syndrome type IIe · CDG-IIe

ORPHA:79333

COG8-CDG

CDG syndrome type IIh · CDG-IIh

ORPHA:95428

Cogan syndrome

ORPHA:1467

Cohen syndrome

ORPHA:193

Congenital muscular dystrophy with intellectual disability and severe epilepsy

CDG syndrome type Iu · CDG-Iu

ORPHA:329178

Cooks syndrome

Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges syndrome · ODP

ORPHA:1487

DDOST-CDG

CDG syndrome type Ir · CDG-Ir

ORPHA:300536

DK1-CDG

Dolichol kinase deficiency · Hypotonia and ichthyosis due to dolichol phosphate deficiency

ORPHA:91131

DPAGT1-CDG

CDG syndrome type Ij · CDG-Ij

ORPHA:86309

DPM1-CDG

CDG syndrome type Ie · CDG-Ie

ORPHA:79322

DPM3-CDG

CDG syndrome type Io · CDG-Io

ORPHA:263494

Feingold syndrome type 1

Brunner-Winter syndrome type 1 · Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1

ORPHA:391641

Feingold syndrome type 2

Brachydactyly-short stature-microcephaly syndrome · Brunner-Winter syndrome type 2

ORPHA:391646