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 ×

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

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-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome

Hamamy syndrome

ORPHA:314555

FATCO syndrome

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

ORPHA:2492

Female restricted epilepsy with intellectual disability

Juberg-Hellman syndrome · EFMR

ORPHA:101039

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

Frank-Ter Haar syndrome

Ter Haar syndrome

ORPHA:137834

Fraser syndrome

Cryptophthalmos-syndactyly syndrome

ORPHA:2052

Frasier syndrome

ORPHA:347

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

Haddad syndrome

Congenital central alveolar hypoventilation-Hirschsprung disease syndrome · Ondine-Hirschsprung disease

ORPHA:99803

HANAC syndrome

Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome · Hereditary angiopathy-nephropathy-aneurysms-muscle cramps syndrome

ORPHA:73229

HARP syndrome

Hypoprebetalipoproteinemia-acanthocytosis-retinitis pigmentosa-pallidal degeneration syndrome

ORPHA:157855

Harrod syndrome

Cranio-facio-digito-genital syndrome

ORPHA:2115

Heart-hand syndrome

Atriodigital dysplasia

ORPHA:228184

HEC syndrome

Hydrocephalus-endocardial fibroelastosis-cataract syndrome

ORPHA:2119

Heiner syndrome

Cow's milk-induced pulmonary hypersensitivity syndrome

ORPHA:99932

HELLP syndrome

Hemolysis, elevated liver enzymes, low platelets in pregnancy · Hemolysis-elevated liver enzymes-low platelets syndrome

ORPHA:244242

Hemiconvulsion-hemiplegia-epilepsy syndrome

HHE · HHE syndrome

ORPHA:86908

Hemidystonia-hemiatrophy syndrome

HD-HA syndrome

ORPHA:306741

Hemiparkinsonism-hemiatrophy syndrome

HP-HA syndrome

ORPHA:306669

Hennekam syndrome

Lymphedema-lymphangiectasia-intellectual disability syndrome

ORPHA:2136

HERNS syndrome

Hereditary endotheliopathy-retinopathy-nephropathy-stroke syndrome

ORPHA:63261

HIDEA syndrome

Severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome

ORPHA:436141

Hinman syndrome

HAS · HS

ORPHA:84085

Holmes-Adie syndrome

Tonic pupil-tendon areflexia syndrome · Adie syndrome

ORPHA:454718

Huriez syndrome

Palmoplantar keratoderma-sclerodactyly syndrome · Palmoplantar hyperkeratosis-sclerodactyly syndrome

ORPHA:384

Hurler syndrome

Hurler disease · MPS1H

ORPHA:93473

Hurler-Scheie syndrome

MPS1H/S · MPSIH/S

ORPHA:93476

Hyper-IgE syndrome

ORPHA:331223

Hyperimmunoglobulinemia D with periodic fever

HIDS · Hyper-IgD syndrome

ORPHA:343

Hyperinsulinism-hyperammonemia syndrome

HI/HA syndrome

ORPHA:35878

Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

HHH syndrome · ORNT1 deficiency

ORPHA:415

Hypertelorism-microtia-facial clefting syndrome

Bixler-Christian-Gorlin syndrome · HMC syndrome

ORPHA:2213

Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome

HUPRA syndrome

ORPHA:363694

Hypoglossia-hypodactyly syndrome

Aglossia-adactylia syndrome · Hanhart syndrome

ORPHA:989

Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome

HELIX syndrome

ORPHA:528105

Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome

HEDH syndrome · ANOTHER syndrome

ORPHA:1882

Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome

4H syndrome

ORPHA:88637