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"

152 matching diseasesClear search ×

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

Microphthalmia with linear skin defects syndrome

MCOPS7 · MIDAS syndrome

ORPHA:2556

Monosomy 18p syndrome

18p- syndrome · De Grouchy syndrome type 1

ORPHA:1598

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

Neurogenic scapuloperoneal syndrome, Kaeser type

Kaeser syndrome · Stark-Kaeser syndrome

ORPHA:85146

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

Oguchi disease

Congenital stationary night blindness, Oguchi type · Oguchi syndrome

ORPHA:75382

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

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

Pai syndrome

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

ORPHA:1993

Pallister-Killian syndrome

Isochromosome 12p mosaicism · Isochromosome 12p syndrome

ORPHA:884

Pelvis-shoulder dysplasia

Kosenow syndrome · Scapuloiliac dysostosis

ORPHA:2839

POEMS syndrome

Crow-Fukase syndrome · Osteosclerotic myeloma

ORPHA:2905

Progressive supranuclear palsy

PSP syndrome

ORPHA:683

Right isomerism

Ivemark syndrome · Right atrial isomerism

ORPHA:97548

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

Sanjad-Sakati syndrome

HRD syndrome · Hypoparathyroidism-intellectual disability-dysmorphism syndrome

ORPHA:2323

Schimke immuno-osseous dysplasia

Schimke syndrome · Spondyloepiphyseal dysplasia-nephrotic syndrome

ORPHA:1830

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

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

SLC12A2-related autosomal recessive neonatal-developmental delay-intellectual disability-feeding difficulty-sensorineural deafness syndrome

Kilquist syndrome

ORPHA:633021

Smith-Lemli-Opitz syndrome

7-dehydrocholesterol reductase deficiency · RSH syndrome

ORPHA:818

Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome

SINO syndrome

ORPHA:521390

Syndactyly-telecanthus-anogenital and renal malformations syndrome

STAR syndrome

ORPHA:140952

Takenouchi-Kosaki syndrome

Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome

ORPHA:487796

Tarsal kink syndrome

ORPHA:99170

Thrombocytopenia-absent radius syndrome

TAR syndrome

ORPHA:3320

Tricho-dento-osseous syndrome

TDO syndrome

ORPHA:3352