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"

143 matching diseasesClear search ×

Neuromyelitis optica spectrum disorder

Devic disease · Devic syndrome

ORPHA:71211

Neuromyelitis optica spectrum disorder with anti-AQP4 antibodies

Devic disease · Devic syndrome

ORPHA:592850

Neuromyelitis optica spectrum disorder with anti-MOG antibodies

Devic disease · Devic syndrome

ORPHA:592856

Neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies

Devic disease · Devic syndrome

ORPHA:592869

Nodulosis-arthropathy-osteolysis syndrome

NAO syndrome

ORPHA:85196

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

CBL syndrome · Noonan syndrome-like disorder with JMML

ORPHA:363972

Okamoto syndrome

ORPHA:2729

Ophthalmomandibulomelic dysplasia

OMM syndrome · Pillay syndrome

ORPHA:2741

Opsoclonus-myoclonus syndrome

Ataxo-opso-myoclonus syndrome · Dancing eye syndrome

ORPHA:1183

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

POEMS syndrome

Crow-Fukase syndrome · Osteosclerotic myeloma

ORPHA:2905

Primary cutaneous T-cell lymphoma

CTCL · Mycosis fungoides

ORPHA:171901

Progressive hemifacial atrophy

Hemifacial atrophy · PHA

ORPHA:1214

Progressive supranuclear palsy

PSP syndrome

ORPHA:683

Proteus syndrome

Partial gigantism-nevi-hemihypertrophy-macrocephaly syndrome

ORPHA:744

Ring chromosome 1 syndrome

Ring chromosome 1 · Ring 1

ORPHA:1437

Ring chromosome 4 syndrome

Ring chromosome 4 · Ring 4

ORPHA:1447

Ring chromosome 8 syndrome

Ring chromosome 8 · Ring 8

ORPHA:1450

Rotor syndrome

Hyperbilirubinemia, Rotor type

ORPHA:3111

Sanjad-Sakati syndrome

HRD syndrome · Hypoparathyroidism-intellectual disability-dysmorphism syndrome

ORPHA:2323

Schwartz-Jampel syndrome

Aberfeld syndrome · Burton skeletal dysplasia

ORPHA:800

Seckel syndrome

ORPHA:808

Seizures-scoliosis-macrocephaly syndrome

SSM syndrome

ORPHA:466926

Semicircular canal dehiscence syndrome

SCD syndrome

ORPHA:420402

SERKAL syndrome

Sex reversion-kidneys, adrenal and lung dysgenesis syndrome

ORPHA:139466

Serpentine fibula-polycystic kidneys syndrome

Exner syndrome

ORPHA:2853

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

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

Sotos syndrome

Cerebral gigantism

ORPHA:821

Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome

SINO syndrome

ORPHA:521390

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

Triple A syndrome

2A syndrome · 3A syndrome

ORPHA:869

Trisomy X syndrome

47,XXX syndrome · Triplo-X syndrome

ORPHA:3375

Turner syndrome

45,X syndrome · 45,X/46,XX syndrome

ORPHA:881

Visceral heterotaxy

Heterotaxy syndrome · HTX

ORPHA:450

W syndrome

Pallister-W syndrome

ORPHA:2804

Wagner disease

Dominant hyaloideoretinal dystrophy of Wagner · VCAN-related vitreoretinopathy

ORPHA:898

Werner syndrome

Adult progeria · WS

ORPHA:902

Wolf-Hirschhorn syndrome

4p- syndrome · Distal deletion 4p

ORPHA:280

XK aprosencephaly syndrome

Garcia-Lurie syndrome · XK syndrome

ORPHA:3469