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 ×

Microphthalmia-brain atrophy syndrome

MCOPS10 · MOBA syndrome

ORPHA:77299

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 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

Nager syndrome

Mandibulofacial dysostosis with preaxial limb anomalies · NAFD

ORPHA:245

NAME syndrome

Nevi-atrial myxoma-myxoid neurofibromata-ephelides syndrome

ORPHA:623

NARP syndrome

Neurogenic muscle weakness-ataxia-retinitis pigmentosa syndrome · Neuropathy-ataxia-retinitis pigmentosa syndrome

ORPHA:644

Naxos disease

KWWH type I · Keratoderma with woolly hair type I

ORPHA:34217

Nelson syndrome

ORPHA:199244

Neonatal ichthyosis-sclerosing cholangitis syndrome

Ichthyosis-hypotrichosis-sclerosing cholangitis syndrome · IHSC

ORPHA:59303

NESCAV syndrome

Neurodegeneration-spasticity-cerebellar atrophy-cortical visual impairment syndrome

ORPHA:662367

NEVADA syndrome

Nevus epidermicus verrucosus with angiodysplasia and aneurysms

ORPHA:370059

Nevo syndrome

Cerebral gigantism, Nevo type

ORPHA:2691

Nicolau syndrome

Embolia cutis medicamentosa · Livedo-like dermatitis

ORPHA:664787

NOCARH syndrome

Neonatal-onset cytopenia-autoinflammation-rash episodes of hemophagocytic lymphohistiocytosis syndrome · Neonatal-onset cytopenia-autoinflammation-rash episodes of HLH syndrome

ORPHA:619363

Nodulosis-arthropathy-osteolysis syndrome

NAO syndrome

ORPHA:85196

Noonan syndrome

ORPHA:648

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

CBL syndrome · Noonan syndrome-like disorder with JMML

ORPHA:363972

Null syndrome

PLP1 null syndrome · Pelizaeus-Merzbacher disease, null syndrome

ORPHA:280234

Oculocerebrorenal syndrome of Lowe

Lowe disease · Lowe oculo-cerebro-renal syndrome

ORPHA:534

Oculodentodigital dysplasia

Oculo-dento-digital dysplasia · ODOD syndrome

ORPHA:2710

Oculogastrointestinal-neurodevelopmental syndrome

OGIN Syndrome

ORPHA:611201

Oculotrichoanal syndrome

MOTA syndrome · Manitoba oculotrichoanal syndrome

ORPHA:2717

Oley syndrome

Congenital hypotrichosis-milia syndrome

ORPHA:79458

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

Osteosclerotic bone dysplasia

Raine syndrome

ORPHA:1832

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

Painful legs and moving toes syndrome

PLMT syndrome

ORPHA:617440

PASS syndrome

Pyoderma gangrenosum-acne-hidradenitis suppurativa-ankylosing spondylitis syndrome

ORPHA:641385

PEHO syndrome

Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy

ORPHA:2836

POEMS syndrome

Crow-Fukase syndrome · Osteosclerotic myeloma

ORPHA:2905

Port-wine nevi-mega cisterna magna-hydrocephalus syndrome

Nova syndrome

ORPHA:2703

Primary basilar invagination

Bull-Nixon syndrome

ORPHA:2285

Progressive hemifacial atrophy

Hemifacial atrophy · PHA

ORPHA:1214

Progressive supranuclear palsy

PSP syndrome

ORPHA:683

Proteasome-associated autoinflammatory syndrome

ALDD syndrome · Autoinflammation-lipodystrophy-dermatosis syndrome

ORPHA:324977

Proximal myotonic myopathy

Myotonic dystrophy type 2 · Proximal myotonic dystrophy

ORPHA:606

Ramon syndrome

Cherubism-gingival fibromatosis-intellectual disability syndrome

ORPHA:3019