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 ×

Monosomy 18q syndrome

18q- syndrome · Deletion 18q

ORPHA:1600

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

Muscle-eye-brain disease

MEB syndrome · Muscle-eye-brain syndrome

ORPHA:588

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

5q- syndrome · MDS

ORPHA:86841

N syndrome

ORPHA:2608

Naegeli-Franceschetti-Jadassohn syndrome

NFJ syndrome · Naegeli syndrome

ORPHA:69087

NAME syndrome

Nevi-atrial myxoma-myxoid neurofibromata-ephelides syndrome

ORPHA:623

Neurofaciodigitorenal syndrome

Freire Maia-Pinheiro-Opitz syndrome

ORPHA:2673

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

Oculocerebral hypopigmentation syndrome, Cross type

Cross syndrome

ORPHA:2719

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

Pelviscapular dysplasia

Cousin syndrome · Familial pelvis-scapular dysplasia

ORPHA:93333

POEMS syndrome

Crow-Fukase syndrome · Osteosclerotic myeloma

ORPHA:2905

Primary Fanconi renotubular syndrome

Primary Fanconi renal syndrome · DeToni-Debré-Fanconi syndrome

ORPHA:3337

Progressive non-infectious anterior vertebral fusion

PAVF · Copenhagen syndrome

ORPHA:2062

Progressive supranuclear palsy

PSP syndrome

ORPHA:683

Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome

Cerebrorenal syndrome, Perez type

ORPHA:505242

Pyknoachondrogenesis

Camera syndrome

ORPHA:3003

Radio-renal syndrome

ORPHA:3015

Renal coloboma syndrome

Coloboma of optic nerve with renal disease · Papillo-renal syndrome

ORPHA:1475

Renal nutcracker syndrome

Left renal vein entrapment syndrome · RNS

ORPHA:71273

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

RNU4-2-related autosomal dominant neurodevelopmental disorder

ReNU syndrome

ORPHA:686488

Sanjad-Sakati syndrome

HRD syndrome · Hypoparathyroidism-intellectual disability-dysmorphism syndrome

ORPHA:2323

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

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

Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome

SINO syndrome

ORPHA:521390

Spinal arteriovenous metameric syndrome

Cutaneomeningospinal angiomatosis · SAMS 1-31

ORPHA:53721

Syndactyly-telecanthus-anogenital and renal malformations syndrome

STAR syndrome

ORPHA:140952

Thrombocytopenia-absent radius syndrome

TAR syndrome

ORPHA:3320

Thyrocerebrorenal syndrome

Cutler-Bass-Romshe syndrome

ORPHA:3327

Townes-Brocks syndrome

Sensorineural hearing loss with imperforate anus and hypoplastic thumbs · REAR syndrome

ORPHA:857

Tricho-dento-osseous syndrome

TDO syndrome

ORPHA:3352