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 ×

Netherton syndrome

Bamboo hair syndrome · Comèl-Netherton syndrome

ORPHA:634

Nevo syndrome

Cerebral gigantism, Nevo type

ORPHA:2691

Nodulosis-arthropathy-osteolysis syndrome

NAO syndrome

ORPHA:85196

Noonan syndrome

ORPHA:648

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

CBL syndrome · Noonan syndrome-like disorder with JMML

ORPHA:363972

Ocular anomalies-axonal neuropathy-developmental delay syndrome

Harel-Yoon syndrome

ORPHA:496790

Oculodentodigital dysplasia

Oculo-dento-digital dysplasia · ODOD syndrome

ORPHA:2710

Oculogastrointestinal-neurodevelopmental syndrome

OGIN Syndrome

ORPHA:611201

Oculotrichoanal syndrome

MOTA syndrome · Manitoba oculotrichoanal syndrome

ORPHA:2717

Ophthalmomandibulomelic dysplasia

OMM syndrome · Pillay syndrome

ORPHA:2741

Opsoclonus-myoclonus syndrome

Ataxo-opso-myoclonus syndrome · Dancing eye syndrome

ORPHA:1183

Orofaciodigital syndrome type 2

Mohr syndrome · OFD2

ORPHA:2751

Orofaciodigital syndrome type 3

OFD3 · Oral-facial-digital syndrome type 3

ORPHA:2752

Orofaciodigital syndrome type 7

OFD7 · Oral-facial-digital syndrome type 7

ORPHA:90649

Otofaciocervical syndrome

Fara-Chlupackova syndrome · OFC syndrome

ORPHA:2792

Pai syndrome

Median cleft of the upper lip-corpus callosum lipoma-midline facial cutaneous polyps syndrome

ORPHA:1993

Perlman syndrome

Nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome

ORPHA:2849

PMP22-RAI1 contiguous gene duplication syndrome

Yuan-Harel-Lupski syndrome · 17p11.2p12 microduplication syndrome

ORPHA:477817

POEMS syndrome

Crow-Fukase syndrome · Osteosclerotic myeloma

ORPHA:2905

Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome

Polyneuropathy-deafness-ataxia-retinitis pigmentosa-cataract syndrome · PHARC syndrome

ORPHA:171848

Port-wine nevi-mega cisterna magna-hydrocephalus syndrome

Nova syndrome

ORPHA:2703

Primary biliary cholangitis

Hanot syndrome · Primary biliary cirrhosis

ORPHA:186

Progressive supranuclear palsy

PSP syndrome

ORPHA:683

Recombinant 8 syndrome

Duplication 8q/deletion 8p · Rec(8) syndrome

ORPHA:96167

Ring chromosome 1 syndrome

Ring chromosome 1 · Ring 1

ORPHA:1437

Ring chromosome 11 syndrome

RC11 · r(11) syndrome

ORPHA:96175

Ring chromosome 4 syndrome

Ring chromosome 4 · Ring 4

ORPHA:1447

Ring chromosome 8 syndrome

Ring chromosome 8 · Ring 8

ORPHA:1450

RNU4-2-related autosomal dominant neurodevelopmental disorder

ReNU syndrome

ORPHA:686488

Roifman syndrome

Spondyloepiphyseal dysplasia-retinal dystrophy-immunodeficiency syndrome

ORPHA:353298

Sanjad-Sakati syndrome

HRD syndrome · Hypoparathyroidism-intellectual disability-dysmorphism syndrome

ORPHA:2323

Scimitar syndrome

Congenital pulmonary venolobar syndrome · Epibronchial right pulmonary vein syndrome

ORPHA:185

Seizures-scoliosis-macrocephaly syndrome

SSM syndrome

ORPHA:466926

Semicircular canal dehiscence syndrome

SCD syndrome

ORPHA:420402

Severe dermatitis-multiple allergies-metabolic wasting syndrome

Congenital erythroderma-hypotrichosis-recurrent infections-multiple food allergies syndrome · SAM syndrome

ORPHA:369992

Severe oculo-renal-cerebellar syndrome

Hunter-Jurenka-Thompson syndrome · Oculorenocerebellar syndrome

ORPHA:2715

Sheehan syndrome

ORPHA:91355

Sheldon-Hall syndrome

SSH · DA2B

ORPHA:1147

Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome

SAMS syndrome

ORPHA:397623

Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome

SOFT syndrome

ORPHA:314394

Short stature-optic atrophy-Pelger-Huët anomaly syndrome

SOPH syndrome

ORPHA:391677

Smith-Lemli-Opitz syndrome

7-dehydrocholesterol reductase deficiency · RSH syndrome

ORPHA:818

Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome

SINO syndrome

ORPHA:521390

Structural heart defects-renal anomalies syndrome

Severe congenital heart defects-renal anomalies syndome · SHDRA syndrome

ORPHA:689822

Symphalangism with multiple anomalies of hands and feet

Learman syndrome

ORPHA:3246

Syndactyly-telecanthus-anogenital and renal malformations syndrome

STAR syndrome

ORPHA:140952

Thrombocytopenia-absent radius syndrome

TAR syndrome

ORPHA:3320

Tricho-dento-osseous syndrome

TDO syndrome

ORPHA:3352