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"

161 matching diseasesClear search ×

Dent disease

Dent syndrome · Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis

ORPHA:1652

Denys-Drash syndrome

Wilms tumor-DSD syndrome · Drash syndrome

ORPHA:220

Desbuquois syndrome

Desbuquois dysplasia · DBQD

ORPHA:1425

Developmental and epileptic encephalopathy with spike-wave activation in sleep

CSWS · CSWSS syndrome

ORPHA:725

Diethylstilbestrol syndrome

DES embryofetopathy · DES syndrome

ORPHA:1916

Digitorenocerebral syndrome

DRC syndrome · Eronen-Somer-Gustafsson syndrome

ORPHA:1674

Dilated cardiomyopathy with ataxia

3-methylglutaconic aciduria type 5 · DCMA syndrome

ORPHA:66634

Distal deletion 3p syndrome

3p- syndrome · Distal monosomy 3p

ORPHA:1620

Dobrow syndrome

Syngnathia-multiple anomalies syndrome

ORPHA:3262

DOORS syndrome

Deafness-onychodystrophy-osteodystrophy-intellectual disability-seizures syndrome · Autosomal recessive deafness-onychodystrophy syndrome

ORPHA:79500

Down syndrome

Trisomy 21

ORPHA:870

Dravet syndrome

SMEI · Severe myoclonic epilepsy of infancy

ORPHA:33069

Drug reaction with eosinophilia and systemic symptoms

DRESS syndrome · Drug rash with eosinophilia and systemic symptoms

ORPHA:139402

Duane retraction syndrome

DRS · DURS

ORPHA:233

Duplication of the pituitary gland

DPG-plus syndrome · Duplication of the pituitary gland-plus syndrome

ORPHA:314621

Dursun syndrome

Pulmonary arterial hypertension-leukopenia-atrial septal defect syndrome

ORPHA:178503

DYRK1A-related intellectual disability syndrome

DYRK1A syndrome

ORPHA:464306

Epilepsy with myoclonic-atonic seizures

Doose syndrome · EMAS

ORPHA:1942

Epiphyseal dysplasia-hearing loss-dysmorphism syndrome

Finucane-Kurtz-Scott syndrome · Epiphyseal dysplasia-deafness-dysmorphism syndrome

ORPHA:1825

Febrile infection-related epilepsy syndrome

AERRPS · Acute encephalitis with refractory repetitive partial seizures

ORPHA:163703

Fibular aplasia-complex brachydactyly syndrome

Du Pan syndrome

ORPHA:2639

Frey syndrome

Baillarger syndrome · Auriculotemporal syndrome

ORPHA:662240

Generalized resistance to thyroid hormone

Deafness-thyroid hormone resistance syndrome · Refetoff syndrome

ORPHA:3221

Gingival fibromatosis-progressive deafness syndrome

Jones syndrome · Gingival fibromatosis-progressive hearing loss syndrome

ORPHA:2027

Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome

GEMSS syndrome

ORPHA:2084

H syndrome

ORPHA:168569

HIDEA syndrome

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

ORPHA:436141

High myopia-sensorineural deafness syndrome

High myopia-sensorineural hearing loss syndrome

ORPHA:363396

Hirschsprung disease-deafness-polydactyly syndrome

Hirschsprung disease-hearing loss-polydactyly syndrome · Santos-Mateus-Leal syndrome

ORPHA:2155

Hyperzincemia and hypercalprotectinemia

PSTPIP1-associated myeloid-related proteinemia inflammatory syndrome · PAMI syndrome

ORPHA:251523

Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome

4H syndrome

ORPHA:88637

Hypotrichosis-deafness syndrome

Hypotrichosis-hearing loss syndrome

ORPHA:330029

Jervell and Lange-Nielsen syndrome

Long QT interval-deafness syndrome · Long QT interval-hearing loss syndrome

ORPHA:90647

Johnson neuroectodermal syndrome

Alopecia-anosmia-deafness-hypogonadism syndrome · Johnson-McMillin syndrome

ORPHA:2316

Keratoderma hereditarium mutilans

Mutilating keratoderma plus hearing loss · Mutilating keratoderma of Vohwinkel

ORPHA:494

L1 syndrome

CRASH syndrome · Corpus callosum hypoplasia-retardation-adducted thumbs-spasticity-hydrocephalus syndrome

ORPHA:275543

Laryngeal abductor paralysis-intellectual disability syndrome

Plott syndrome

ORPHA:2375

LUMBAR syndrome

PELVIS syndrome · Perineal hemangioma-external genitalia malformations-lipomyelomeningocele-vesicorenal abnormalities-imperforate anus-skin tag syndrome

ORPHA:83628

MASS syndrome

Mitral valve-aorta-skeleton-skin syndrome

ORPHA:99715

Matthew-Wood syndrome

Spear syndrome · Anophthalmia-pulmonary hypoplasia syndrome

ORPHA:2470

Mohr-Tranebjaerg syndrome

DDON syndrome · Deafness-dystonia-optic neuronopathy syndrome

ORPHA:52368

Monosomy 9p syndrome

9p deletion syndrome · 9p- syndrome

ORPHA:261112

Multiple endocrine neoplasia type 2A

MEN2A · PTC syndrome

ORPHA:247698

Multiple synostoses syndrome

Deafness-Hermann type symphalangism syndrome · Facio-audio-symphalangism

ORPHA:3237

Musculocontractural Ehlers-Danlos syndrome

Musculocontractural EDS · mcEDS

ORPHA:2953

Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality

5q- syndrome · MDS

ORPHA:86841

Myoclonus-cerebellar ataxia-deafness syndrome

Myoclonus-cerebellar ataxia-hearing loss syndrome

ORPHA:2589

N syndrome

ORPHA:2608