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"

184 matching diseasesClear search ×

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

MEGDEL syndrome

3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome · 3-methylglutaconic aciduria with hearing loss-encephalopathy-Leigh-like syndrome

ORPHA:352328

MEHMO syndrome

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

ORPHA:85282

Meigs syndrome

Demons-Meigs syndrome

ORPHA:314451

Melhem-Fahl syndrome

ORPHA:2482

Melnick-Needles syndrome

Melnick-Needles osteodysplasty

ORPHA:2484

Melorheostosis with osteopoikilosis

MSBD syndrome · Mixed sclerosing bone dystrophy

ORPHA:1879

MEND syndrome

Male EBP disorder with neurological defects

ORPHA:401973

Menkes disease

Menkes kinky hair disease · MD

ORPHA:565

MEPAN syndrome

Mitochondrial enoyl CoA reductase protein-associated neurodegeneration syndrome · Autosomal recessive childhood-onset dystonia, DYT29 type

ORPHA:508093

Michels syndrome

3MC1 syndrome · Oculopalatoskeletal syndrome

ORPHA:2506

Micro syndrome

WARBM · Warburg micro syndrome

ORPHA:2510

Microcephaly-capillary malformation syndrome

MIC-CAP syndrome · MIC-CM syndrome

ORPHA:294016

Microcornea-myopic chorioretinal atrophy-telecanthus syndrome

MMCAT syndrome

ORPHA:369970

Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome

MPPC syndrome

ORPHA:231736

Microphthalmia with linear skin defects syndrome

MCOPS7 · MIDAS syndrome

ORPHA:2556

Microphthalmia-brain atrophy syndrome

MCOPS10 · MOBA syndrome

ORPHA:77299

Mietens syndrome

Intellectual disability, Mietens-Weber type

ORPHA:2557

Mills syndrome

ORPHA:94091

MIRAGE syndrome

Myelodysplasia-infection-restriction of growth-adrenal hypoplasia-genital anomalies-enteropathy syndrome · Myelodysplasia-infection-restriction of growth-adrenal hypoplasia-genital phenotypes-enteropathy syndrome

ORPHA:494433

Mirizzi syndrome

Extrinsic biliary compression syndrome

ORPHA:521219

MMEP syndrome

MCOPS8 · Microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome

ORPHA:3434

Moebius syndrome

Möbius syndrome

ORPHA:570

MOMO syndrome

Macrocephaly-obesity-intellectual disability-ocular abnormalities syndrome · Macrosomia-obesity-macrocephaly-ocular abnormalities syndrome

ORPHA:2563

Monosomy 18p syndrome

18p- syndrome · De Grouchy syndrome type 1

ORPHA:1598

Monosomy 18q syndrome

18q- syndrome · Deletion 18q

ORPHA:1600

Monosomy 22 syndrome

Del(22) · Deletion 22

ORPHA:96123

Monosomy 5p syndrome

Cri du chat syndrome · Deletion 5p

ORPHA:281

Monosomy 9p syndrome

9p deletion syndrome · 9p- syndrome

ORPHA:261112

Monosomy X syndrome

ORPHA:99226

MORM syndrome

Intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome

ORPHA:75858

Morning glory disc anomaly

Morning glory syndrome · Ectasic coloboma

ORPHA:35737

Morvan syndrome

Limbic encephalitis-neuromyotonia-hyperhidrosis-polyneuropathy syndrome · Morvan fibrillary chorea

ORPHA:83467

Moynahan syndrome

Alopecia-epilepsy-intellectual disability syndrome, Moynahan type

ORPHA:2574

MRCS syndrome

Microcornea-rod-cone dystrophy-cataract-posterior staphyloma syndrome

ORPHA:263347

Muenke syndrome

ORPHA:53271

Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome

MARCH syndrome

ORPHA:500135

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

Myhre syndrome

Myhre-Laryngotracheal stenosis-arthropathy-prognathism-short stature syndrome · Facial dysmorphism-intellectual disability-short stature-hearing loss syndrome

ORPHA:2588

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

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

Oculotrichoanal syndrome

MOTA syndrome · Manitoba oculotrichoanal syndrome

ORPHA:2717