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 ×

Craniosynostosis-anal anomalies-porokeratosis syndrome

CAP syndrome · CDAGS syndrome

ORPHA:85199

Curly hair-acral keratoderma-caries syndrome

CHAC syndrome · CHACS

ORPHA:307766

Deafness-enamel hypoplasia-nail defects syndrome

Heimler syndrome · Hearing loss-enamel hypoplasia-nail defects syndrome

ORPHA:3220

Deafness-lymphedema-leukemia syndrome

Hearing loss-lymphedema-leukemia syndrome · Emberger syndrome

ORPHA:3226

Diethylstilbestrol syndrome

DES embryofetopathy · DES syndrome

ORPHA:1916

Digitorenocerebral syndrome

DRC syndrome · Eronen-Somer-Gustafsson syndrome

ORPHA:1674

Distal deletion 3p syndrome

3p- syndrome · Distal monosomy 3p

ORPHA:1620

Double uterus-hemivagina-renal agenesis syndrome

Double uterus and obstructed hemivagina syndrome · OHVIRA syndrome

ORPHA:3411

Dysequilibrium syndrome

CAMRQ syndrome · Non-progressive cerebellar ataxia-intellectual disability syndrome

ORPHA:1766

EAST syndrome

Epilepsy-ataxia-sensorineural hearing loss-tubulopathy syndrome · SeSAME syndrome

ORPHA:199343

Ectrodactyly-cleft palate syndrome

ECP syndrome

ORPHA:1889

EDICT syndrome

Autosomal dominant keratoconus with early-onset anterior polar cataracts · Endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning syndrome

ORPHA:293936

EEC syndrome

Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome

ORPHA:1896

EEM syndrome

Ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome

ORPHA:1897

Ehlers-Danlos/osteogenesis imperfecta syndrome

EDS/OI syndrome

ORPHA:230857

Eiken syndrome

ORPHA:79106

Emanuel syndrome

Der(22)t(11;22) syndrome · Supernumerary der(22) syndrome

ORPHA:96170

EN1-related dorsoventral syndrome

ENDOVES · ENDOVE syndrome

ORPHA:611223

Endocrine-cerebro-osteodysplasia syndrome

ECO syndrome

ORPHA:199332

Eng-Strom syndrome

Short stature-locking fingers syndrome

ORPHA:1937

Epstein syndrome

Alport syndrome with macrothrombocytopenia

ORPHA:1019

Erythrokeratodermia-cardiomyopathy syndrome

EKC syndrome

ORPHA:476096

Evans syndrome

Autoimmune hemolytic anemia and autoimmune thrombocytopenia · Immune pancytopenia

ORPHA:1959

Fechtner syndrome

Alport syndrome with leukocyte inclusions and macrothrombocytopenia

ORPHA:1984

Feingold syndrome

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

ORPHA:1305

Focal facial dermal dysplasia type I

Bitemporal aplasia cutis congenita · Brauer syndrome

ORPHA:79133

Fowler urethral sphincter dysfunction syndrome

Fowler-Christmas-Chapple syndrome · Fowler syndrome

ORPHA:2795

Fraser syndrome

Cryptophthalmos-syndactyly syndrome

ORPHA:2052

Frasier syndrome

ORPHA:347

Frey syndrome

Baillarger syndrome · Auriculotemporal syndrome

ORPHA:662240

GAPO syndrome

Growth delay-alopecia-pseudoanodontia-optic atrophy syndrome

ORPHA:2067

Gardner syndrome

ORPHA:79665

GMS syndrome

Goniodysgenesis-intellectual disability-short stature syndrome

ORPHA:2090

Gorlin-Chaudhry-Moss syndrome

Craniofacial dysostosis-genital, dental, cardiac anomalies syndrome · Cranofacial dysostosis-hypertrichosis-hypoplasia of labia majora syndrome

ORPHA:2095

H syndrome

ORPHA:168569

HARP syndrome

Hypoprebetalipoproteinemia-acanthocytosis-retinitis pigmentosa-pallidal degeneration syndrome

ORPHA:157855

HEC syndrome

Hydrocephalus-endocardial fibroelastosis-cataract syndrome

ORPHA:2119

Heiner syndrome

Cow's milk-induced pulmonary hypersensitivity syndrome

ORPHA:99932

Hemiconvulsion-hemiplegia-epilepsy syndrome

HHE · HHE syndrome

ORPHA:86908

Hurler syndrome

Hurler disease · MPS1H

ORPHA:93473

Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

HHH syndrome · ORNT1 deficiency

ORPHA:415

Hypertelorism-microtia-facial clefting syndrome

Bixler-Christian-Gorlin syndrome · HMC syndrome

ORPHA:2213

Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome

HEDH syndrome · ANOTHER syndrome

ORPHA:1882

Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome

4H syndrome

ORPHA:88637

Hypoparathyroidism-sensorineural deafness-renal disease syndrome

Hypoparathyroidism-sensorineural hearing loss-renal disease syndrome · Barakat syndrome

ORPHA:2237

IBIDS syndrome

Tay syndrome · Trichothiodystrophy type E

ORPHA:453

ICF syndrome

Immunodeficiency-centromeric instability-facial dysmorphism syndrome · Immunodeficiency-centromeric instability-facial anomalies syndrome

ORPHA:2268

Iridocorneal endothelial syndrome

ICE syndrome

ORPHA:64734