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"

187 matching diseasesClear search ×

OBSOLETE: Spondylocostal dysostosis-anal atresia-genitourinary malformation syndrome

OBSOLETE: Casamassima-Morton-Nance syndrome

ORPHA:94095

OBSOLETE: Sporadic Leigh syndrome

OBSOLETE: Sporadic Leigh disease · OBSOLETE: Sporadic infantile subacute necrotizing encephalopathy

ORPHA:255199

OBSOLETE: Syndromes with synostoses of limbs

ORPHA:294961

OBSOLETE: Syndromic frontonasal dysplasia

OBSOLETE: Syndromic median cleft syndrome

ORPHA:391479

OBSOLETE: Syndromic inherited retinal disorder

OBSOLETE: Syndromic retinal dystrophy

ORPHA:519325

OBSOLETE: Syndromic lymphedema

ORPHA:89832

OBSOLETE: Syndromic macular dystrophy

ORPHA:519323

OBSOLETE: Syndromic myopia

ORPHA:98620

OBSOLETE: Syndromic rod-cone dystrophy

OBSOLETE: Syndromic retinitis pigmentosa

ORPHA:98661

OBSOLETE: Syndromic vitreoretinopathy

ORPHA:519327

OBSOLETE: Taussig-Bing syndrome

ORPHA:101042

OBSOLETE: Torres-Aybar syndrome

ORPHA:3340

OBSOLETE: Tricho-oculo-dermo-vertebral syndrome

OBSOLETE: Ectodermal dysplasia-cataracts-kyphoscoliosis syndrome · OBSOLETE: Alves-dos Santos-Castelo syndrome

ORPHA:3354

OBSOLETE: Trichomegaly-cataract-hereditary spherocytosis syndrome

OBSOLETE: Goldstein-Hutt syndrome

ORPHA:3362

OBSOLETE: True vascular thoracic outlet syndrome

ORPHA:100072

OBSOLETE: Van den Bosch syndrome

ORPHA:3417

OBSOLETE: Van Regemorter-Pierquin-Vamos syndrome

ORPHA:3419

OBSOLETE: X-linked Opitz G/BBB syndrome

OBSOLETE: XLOS · OBSOLETE: X-linked Opitz syndrome

ORPHA:306597

OBSOLETE: Zlotogura-Martinez syndrome

ORPHA:101036

Oculodentodigital dysplasia

Oculo-dento-digital dysplasia · ODOD syndrome

ORPHA:2710

Oculofaciocardiodental syndrome

OFCD syndrome · Cataract-microphthalmia-radiculomegaly-cardiac septal defect syndrome

ORPHA:2712

Oculogastrointestinal-neurodevelopmental syndrome

OGIN Syndrome

ORPHA:611201

Odonto-tricho-ungual-digito-palmar syndrome

OTUDP syndrome · Odonto-tricho-ungual-digito-palmar syndrome, Mendoza-Valiente type

ORPHA:69082

Ogden syndrome

Premature aging appearance-developmental delay-cardiac arrhythmia syndrome

ORPHA:276432

Oley syndrome

Congenital hypotrichosis-milia syndrome

ORPHA:79458

Omenn syndrome

Combined immunodeficiency with hypereosinophilia

ORPHA:39041

Onycho-tricho-dysplasia-neutropenia syndrome

Itin syndrome · ONMR syndrome

ORPHA:2739

Ophthalmomandibulomelic dysplasia

OMM syndrome · Pillay syndrome

ORPHA:2741

Opsoclonus-myoclonus syndrome

Ataxo-opso-myoclonus syndrome · Dancing eye syndrome

ORPHA:1183

OSLAM syndrome

Osteosarcoma-limb anomalies-erythroid macrocytosis syndrome

ORPHA:2760

Otofaciocervical syndrome

Fara-Chlupackova syndrome · OFC syndrome

ORPHA:2792

Otopalatodigital syndrome type 1

OPD I syndrome · OPD syndrome 1

ORPHA:90650

Otopalatodigital syndrome type 2

OPD II syndrome · OPD syndrome 2

ORPHA:90652

Primary biliary cholangitis

Hanot syndrome · Primary biliary cirrhosis

ORPHA:186

Prune belly syndrome

Abdominal muscle deficiency syndrome · Eagle-Barret syndrome

ORPHA:2970

Sanjad-Sakati syndrome

HRD syndrome · Hypoparathyroidism-intellectual disability-dysmorphism syndrome

ORPHA:2323

Severe oculo-renal-cerebellar syndrome

Hunter-Jurenka-Thompson syndrome · Oculorenocerebellar syndrome

ORPHA:2715

Subaortic stenosis-short stature syndrome

Onat syndrome

ORPHA:3191

Trismus-pseudocamptodactyly syndrome

Distal arthrogryposis type 7 · Dutch-Kentucky syndrome

ORPHA:3377

Urofacial syndrome

Hydronephrosis-inverted smile syndrome · Ochoa syndrome

ORPHA:2704

W syndrome

Pallister-W syndrome

ORPHA:2804

Walker-Warburg syndrome

HARD syndrome · Hydrocephalus-agyria-retinal dysplasia syndrome

ORPHA:899

X-linked intellectual disability-cerebellar hypoplasia syndrome

OPHN1 syndrome · Oligophrenin-1 syndrome

ORPHA:137831