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 ×

Hypoparathyroidism-sensorineural deafness-renal disease syndrome

Hypoparathyroidism-sensorineural hearing loss-renal disease syndrome · Barakat syndrome

ORPHA:2237

Hypospadias-intellectual disability, Goldblatt type syndrome

Goldblatt-Wallis syndrome

ORPHA:2261

IBIDS syndrome

Tay syndrome · Trichothiodystrophy type E

ORPHA:453

ICF syndrome

Immunodeficiency-centromeric instability-facial dysmorphism syndrome · Immunodeficiency-centromeric instability-facial anomalies syndrome

ORPHA:2268

Ichthyosis-hypotrichosis syndrome

Hypotrichosis-congenital ichthyosis syndrome · IFAH syndrome

ORPHA:91132

Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome

Baker-Gordon syndrome · SYT1-related neurodevelopmental disorder

ORPHA:522077

Iridocorneal endothelial syndrome

ICE syndrome

ORPHA:64734

JMP syndrome

Joint contractures-muscular atrophy-microcytic anemia-panniculitis-associated lipodystrophy syndrome

ORPHA:324999

Joubert syndrome with hepatic defect

COACH syndrome · Cerebellar vermis hypoplasia-oligophrenia-congenital ataxia-coloboma-hepatic fibrosis

ORPHA:1454

KBG syndrome

Short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome · ANKRD11-related disorder

ORPHA:2332

KID syndrome

KID/HID syndrome · Keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome

ORPHA:477

L1 syndrome

CRASH syndrome · Corpus callosum hypoplasia-retardation-adducted thumbs-spasticity-hydrocephalus syndrome

ORPHA:275543

Laron syndrome

Complete growth hormone insensitivity · GH receptor deficiency

ORPHA:633

Laryngo-onycho-cutaneous syndrome

LOGIC syndrome · Laryngeal and ocular granulation tissue in children from the Indian subcontinent syndrome

ORPHA:2407

LIG4 syndrome

DNA ligase IV deficiency · Ligase 4 syndrome

ORPHA:99812

Linear nevus sebaceus syndrome

Nevus sebaceus of Jadassohn · Nevus sebaceus syndrome

ORPHA:2612

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

MASS syndrome

Mitral valve-aorta-skeleton-skin syndrome

ORPHA:99715

Mayer-Rokitansky-Küster-Hauser syndrome

MRKH syndrome · Rokitansky syndrome

ORPHA:3109

Megacystis-microcolon-intestinal hypoperistalsis syndrome

Berdon syndrome · MMIHS

ORPHA:2241

Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome

MPPH syndrome

ORPHA:83473

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

Microphthalmia with linear skin defects syndrome

MCOPS7 · MIDAS syndrome

ORPHA:2556

Mohr-Tranebjaerg syndrome

DDON syndrome · Deafness-dystonia-optic neuronopathy syndrome

ORPHA:52368

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

NAME syndrome

Nevi-atrial myxoma-myxoid neurofibromata-ephelides syndrome

ORPHA:623

Nelson syndrome

ORPHA:199244

Netherton syndrome

Bamboo hair syndrome · Comèl-Netherton syndrome

ORPHA:634

Nevo syndrome

Cerebral gigantism, Nevo type

ORPHA:2691

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

OBSOLETE: Trichomegaly-cataract-hereditary spherocytosis syndrome

OBSOLETE: Goldstein-Hutt syndrome

ORPHA:3362

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

Odontochondrodysplasia

Chondrodysplasia-dentinogenesis imperfecta-joint laxity syndrome · Goldblatt chondrodysplasia

ORPHA:166272

Ophthalmomandibulomelic dysplasia

OMM syndrome · Pillay syndrome

ORPHA:2741

Opsoclonus-myoclonus syndrome

Ataxo-opso-myoclonus syndrome · Dancing eye syndrome

ORPHA:1183