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 ×

RIN2 syndrome

MACS syndrome · Macrocephaly-alopecia-cutis laxa-scoliosis syndrome

ORPHA:217335

Ring chromosome 1 syndrome

Ring chromosome 1 · Ring 1

ORPHA:1437

Ring chromosome 11 syndrome

RC11 · r(11) syndrome

ORPHA:96175

Ring chromosome 22 syndrome

Ring chromosome 22 · Ring 22

ORPHA:1446

Ring chromosome 4 syndrome

Ring chromosome 4 · Ring 4

ORPHA:1447

Ring chromosome 8 syndrome

Ring chromosome 8 · Ring 8

ORPHA:1450

RNU4-2-related autosomal dominant neurodevelopmental disorder

ReNU syndrome

ORPHA:686488

Rombo syndrome

ORPHA:3110

Sanjad-Sakati syndrome

HRD syndrome · Hypoparathyroidism-intellectual disability-dysmorphism syndrome

ORPHA:2323

SCALP syndrome

Sebaceous nevus-CNS malformations-aplasia cutis congenital-limbal dermoid-pigmented nevus syndrome · Sebaceous nevus-central nervous system malformations-aplasia cutis congenital-limbal dermoid-pigmented nevus syndrome

ORPHA:370052

SCARF syndrome

ORPHA:3134

Seizures-scoliosis-macrocephaly syndrome

SSM syndrome

ORPHA:466926

Semicircular canal dehiscence syndrome

SCD syndrome

ORPHA:420402

Severe dermatitis-multiple allergies-metabolic wasting syndrome

Congenital erythroderma-hypotrichosis-recurrent infections-multiple food allergies syndrome · SAM syndrome

ORPHA:369992

Severe oculo-renal-cerebellar syndrome

Hunter-Jurenka-Thompson syndrome · Oculorenocerebellar syndrome

ORPHA:2715

Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome

SAMS syndrome

ORPHA:397623

Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome

SOFT syndrome

ORPHA:314394

Short stature-optic atrophy-Pelger-Huët anomaly syndrome

SOPH syndrome

ORPHA:391677

SHORT syndrome

Lipodystrophy-Rieger anomaly-diabetes syndrome · Rieger anomaly-partial lipodystrophy syndrome

ORPHA:3163

Smith-Lemli-Opitz syndrome

7-dehydrocholesterol reductase deficiency · RSH syndrome

ORPHA:818

Sotos syndrome

Cerebral gigantism

ORPHA:821

Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome

SINO syndrome

ORPHA:521390

Spinal arteriovenous metameric syndrome

Cutaneomeningospinal angiomatosis · SAMS 1-31

ORPHA:53721

Structural heart defects-renal anomalies syndrome

Severe congenital heart defects-renal anomalies syndome · SHDRA syndrome

ORPHA:689822

Subaortic stenosis-short stature syndrome

Onat syndrome

ORPHA:3191

Sweet syndrome

Acute febrile neutrophilic dermatosis

ORPHA:3243

Syndactyly-telecanthus-anogenital and renal malformations syndrome

STAR syndrome

ORPHA:140952

TAFRO syndrome

Thrombocytopenia-anasarca-fever-renal insufficiency-organomegaly syndrome

ORPHA:457077

TARP syndrome

Pierre Robin sequence-congenital heart defect-talipes syndrome · Pierre Robin syndrome-congenital heart defect-talipes syndrome

ORPHA:2886

Tarsal kink syndrome

ORPHA:99170

TEMPI syndrome

Telangiectasia-erythrocytosis-monoclonal gammopathy-perinephric-fluid collections-intrapulmonary shunting syndrome

ORPHA:284227

Temple syndrome

ORPHA:254516

Temtamy syndrome

Craniofacial dysmorphism-coloboma-corpus callosum agenesis syndrome · Temtamy-Shalash syndrome

ORPHA:1777

Thomas syndrome

Potter sequence-cleft lip/palate-cardiopathy syndrome

ORPHA:3316

Thrombocytopenia-absent radius syndrome

TAR syndrome

ORPHA:3320

Thymoma-hypogammaglobulinemia syndrome

Good syndrome

ORPHA:169105

Tietz syndrome

Hypopigmentation-deafness syndrome · Hypopigmentation-hearing loss syndrome

ORPHA:42665

Timothy syndrome

LQT8 · Long QT syndrome type 8

ORPHA:65283

Townes-Brocks syndrome

Sensorineural hearing loss with imperforate anus and hypoplastic thumbs · REAR syndrome

ORPHA:857

Tremor-ataxia-central hypomyelination syndrome

TACH syndrome

ORPHA:447896

Tricho-dento-osseous syndrome

TDO syndrome

ORPHA:3352

Tricho-retino-dento-digital syndrome

Bork syndrome · Uncombable hair-retinal pigmentary dystrophy-dental anomalies-brachydactyly syndrome

ORPHA:1264

Triphalangeal thumb-polysyndactyly syndrome

TPT-PS syndrome

ORPHA:2950

Triple A syndrome

2A syndrome · 3A syndrome

ORPHA:869

Trisomy X syndrome

47,XXX syndrome · Triplo-X syndrome

ORPHA:3375

Tubulointerstitial nephritis and uveitis syndrome

Dobrin syndrome · TINU syndrome

ORPHA:91500

Tumor necrosis factor receptor 1 associated periodic syndrome

Familial Hibernian fever · TNF receptor 1-associated periodic syndrome

ORPHA:32960

Turner syndrome

45,X syndrome · 45,X/46,XX syndrome

ORPHA:881