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"

80 matching diseasesClear search ×

Morning glory disc anomaly

Morning glory syndrome · Ectasic coloboma

ORPHA:35737

3M syndrome

3-M syndrome · Yakut short stature syndrome

ORPHA:2616

Acropectorovertebral dysplasia

F syndrome

ORPHA:957

Aggressive primary cutaneous T-cell lymphoma

CTCL · Mycosis fungoides

ORPHA:178551

Androgen insensitivity syndrome

AIS · Androgen resistance syndrome

ORPHA:754

Anterior maxillary protrusion-strabismus-intellectual disability syndrome

MRAMS syndrome

ORPHA:562559

Autoimmune polyendocrinopathy type 1

APECED syndrome · APS type 1

ORPHA:3453

Autosomal recessive spastic paraplegia type 21

Mast syndrome · SPG21

ORPHA:101001

Blepharospasm-oromandibular dystonia syndrome

Meige dystonia · Meige syndrome

ORPHA:93964

Bohring-Opitz syndrome

BOS syndrome · Bohring syndrome

ORPHA:97297

Burning mouth syndrome

Stomatopyrosis · BMS

ORPHA:353253

C syndrome

OTCS · Opitz C trigonocephaly

ORPHA:1308

Campomelia, Cumming type

Cumming syndrome

ORPHA:1318

Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy

Maeda syndrome · CARASIL

ORPHA:199354

Choroidal atrophy-alopecia syndrome

Moloney syndrome · Regional choroidal atrophy and alopecia

ORPHA:1433

Colobomatous macrophthalmia-microcornea syndrome

MACOM syndrome

ORPHA:468672

Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome

Mehes syndrome

ORPHA:3038

Familial atypical multiple mole melanoma syndrome

B-K mole syndrome · FAMM-PC syndrome

ORPHA:404560

Feingold syndrome

Brunner-Winter syndrome · Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum

ORPHA:1305

Focal dermal hypoplasia

Goltz syndrome · Goltz-Gorlin syndrome

ORPHA:2092

Galloway-Mowat syndrome

Galloway syndrome · Microcephaly-hiatus hernia-nephrotic syndrome

ORPHA:2065

GAPO syndrome

Growth delay-alopecia-pseudoanodontia-optic atrophy syndrome

ORPHA:2067

Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome

GEMSS syndrome

ORPHA:2084

Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome

GLOW syndrome

ORPHA:404476

GMS syndrome

Goniodysgenesis-intellectual disability-short stature syndrome

ORPHA:2090

Gorlin-Chaudhry-Moss syndrome

Craniofacial dysostosis-genital, dental, cardiac anomalies syndrome · Cranofacial dysostosis-hypertrichosis-hypoplasia of labia majora syndrome

ORPHA:2095

Grant syndrome

ORPHA:2097

H syndrome

ORPHA:168569

Hereditary acrokeratotic poikiloderma

Weary syndrome

ORPHA:2907

Holoprosencephaly-craniosynostosis syndrome

Camero-Lituania-Cohen syndrome · Genoa syndrome

ORPHA:2163

Hyperphosphatasia-intellectual disability syndrome

Mabry syndrome

ORPHA:247262

Indolent primary cutaneous T-cell lymphoma

CTCL · Mycosis fungoides

ORPHA:178548

Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome

MOMES syndrome

ORPHA:397973

Jung syndrome

ORPHA:2321

KLHL7-related Bohring-Opitz-like and Crisponi/Cold-induced sweating-like overlap syndrome

PERCHING syndrome

ORPHA:603684

Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome

Smith-Kingsmore syndrome · MINDS syndrome

ORPHA:457485

MAGIC syndrome

Mouth and genital ulcers-inflamed cartilage syndrome

ORPHA:324972

Mammary-digital-nail syndrome

MDN syndrome · Onycho-digito-mammary syndrome

ORPHA:238744

Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome

MDPL syndrome · MDP syndrome

ORPHA:363649

Mandibulofacial dysostosis-microcephaly syndrome

MFDM syndrome · Mandibulofacial dysostosis, Guion-Almeida type

ORPHA:79113

MASA syndrome

Intellectual disability-aphasia-shuffling gait-adducted thumbs syndrome

ORPHA:2466

MASS syndrome

Mitral valve-aorta-skeleton-skin syndrome

ORPHA:99715

Mayer-Rokitansky-Küster-Hauser syndrome

MRKH syndrome · Rokitansky syndrome

ORPHA:3109

Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome

MPPH syndrome

ORPHA:83473

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

MEHMO syndrome

X-linked intellectual disability-epileptic seizures-hypogenitalism-microcephaly-obesity syndrome

ORPHA:85282

Meigs syndrome

Demons-Meigs syndrome

ORPHA:314451

Melorheostosis with osteopoikilosis

MSBD syndrome · Mixed sclerosing bone dystrophy

ORPHA:1879