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 ×

Digitorenocerebral syndrome

DRC syndrome · Eronen-Somer-Gustafsson syndrome

ORPHA:1674

Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome

Cardiogenital syndrome · Malouf syndrome

ORPHA:2229

Distal deletion 3p syndrome

3p- syndrome · Distal monosomy 3p

ORPHA:1620

Donnai-Barrow syndrome

DBS/FOAR syndrome · Diaphragmatic hernia-exomphalos-hypertelorism syndrome

ORPHA:2143

Double uterus-hemivagina-renal agenesis syndrome

Double uterus and obstructed hemivagina syndrome · OHVIRA syndrome

ORPHA:3411

Ectodermal dysplasia-skin fragility syndrome

McGrath syndrome

ORPHA:158668

Ectrodactyly-cleft palate syndrome

ECP syndrome

ORPHA:1889

EEC syndrome

Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome

ORPHA:1896

EEM syndrome

Ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome

ORPHA:1897

Endocrine-cerebro-osteodysplasia syndrome

ECO syndrome

ORPHA:199332

Erythrokeratodermia-cardiomyopathy syndrome

EKC syndrome

ORPHA:476096

Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome

Friedman-Goodman syndrome · FACES syndrome

ORPHA:1969

Facial dysmorphism-hypertrichosis-epilepsy-intellectual disability/developmental delay-gingival overgrowth syndrome

FHEIG syndrome

ORPHA:598603

Facial dysmorphism-immunodeficiency-livedo-short stature syndrome

FILS syndrome

ORPHA:352712

Facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome

FDLAB syndrome · Facial dysmorphism-lens dislocation-anterior segment abnormalities-nontraumatic conjunctive cysts syndrome

ORPHA:412022

Facial onset sensory and motor neuronopathy

FOSMN syndrome

ORPHA:85162

Familial atypical multiple mole melanoma syndrome

B-K mole syndrome · FAMM-PC syndrome

ORPHA:404560

FATCO syndrome

Hecht-Scott syndrome · Fibular aplasia-tibial campomelia-oligosyndactyly syndrome

ORPHA:2492

Feingold syndrome

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

ORPHA:1305

Felty syndrome

Splenomegaly-neutropenia-rheumatoid arthritis syndrome

ORPHA:47612

Fibrodysplasia ossificans progressiva

FOP · Myositis ossificans progressiva

ORPHA:337

FLOTCH syndrome

Leukonychia totalis-trichilemmal cysts-ciliary dystrophy syndrome

ORPHA:2045

Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome

FHONDA syndrome

ORPHA:397618

Fowler urethral sphincter dysfunction syndrome

Fowler-Christmas-Chapple syndrome · Fowler syndrome

ORPHA:2795

FOXG1 syndrome

FOXG1-related epileptic-dyskinetic encephalopathy

ORPHA:561854

FOXP1 Syndrome

FOXP1-retaled intellectual disability-severe speech delay-mild dysmorphism syndrome

ORPHA:391372

Fragile X syndrome

FRAXA syndrome · FXS

ORPHA:908

Fragile X-associated tremor/ataxia syndrome

FXTAS syndrome

ORPHA:93256

Fraser syndrome

Cryptophthalmos-syndactyly syndrome

ORPHA:2052

FRAXF syndrome

ORPHA:100974

Frey syndrome

Baillarger syndrome · Auriculotemporal syndrome

ORPHA:662240

Fried syndrome

ORPHA:85335

Fryns syndrome

Diaphragmatic hernia-facial dysmorphism-distal limb anomalies syndrome

ORPHA:2059

Furlong syndrome

Marfanoid habitus-craniosynostosis syndrome

ORPHA:97295

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

Growth deficiency-brachydactyly-dysmorphism syndrome

Frias syndrome

ORPHA:2055

H syndrome

ORPHA:168569

HEC syndrome

Hydrocephalus-endocardial fibroelastosis-cataract syndrome

ORPHA:2119

Hemiconvulsion-hemiplegia-epilepsy syndrome

HHE · HHE syndrome

ORPHA:86908

Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

HHH syndrome · ORNT1 deficiency

ORPHA:415

Hyperphosphatasia-intellectual disability syndrome

Mabry syndrome

ORPHA:247262

Hypertelorism-microtia-facial clefting syndrome

Bixler-Christian-Gorlin syndrome · HMC syndrome

ORPHA:2213

Hypocomplementemic urticarial vasculitis

Anti-C1q vasculitis · Mac Duffie hypocomplementemic urticarial vasculitis

ORPHA:36412

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