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 ×

Cataract-nephropathy-encephalopathy syndrome

Crome syndrome

ORPHA:1380

CHIME syndrome

Coloboma-congenital heart disease-ichthyosiform dermatosis-intellectual disability-ear anomalies syndrome · Congenital disorder of glycosylation due to PIGL deficiency

ORPHA:3474

Chronic intestinal pseudoobstruction syndrome

CIPO · CIP syndrome

ORPHA:2978

CK syndrome

X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome

ORPHA:251383

Congenital contractural arachnodactyly

Beals syndrome · Beals-Hecht syndrome

ORPHA:115

Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome

Bassoe syndrome

ORPHA:1875

Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome

SIFD syndrome

ORPHA:369861

Corneodermatoosseous syndrome

CDO syndrome · Stern-Lubinsky-Durrie syndrome

ORPHA:3194

Costello syndrome

FCS syndrome · Faciocutaneoskeletal syndrome

ORPHA:3071

CPE-related Prader-Willi-like syndrome

BDV syndrome · Blakemore-Durmaz-Vasileiou syndrome

ORPHA:633028

Craniosynostosis-anal anomalies-porokeratosis syndrome

CAP syndrome · CDAGS syndrome

ORPHA:85199

Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome

Berant syndrome · Capra-DeMarco syndrome

ORPHA:171839

Curly hair-acral keratoderma-caries syndrome

CHAC syndrome · CHACS

ORPHA:307766

Deafness with labyrinthine aplasia, microtia, and microdontia

Hearing loss with labyrinthine aplasia, microtia, and microdontia · LAMM syndrome

ORPHA:90024

Dent disease

Dent syndrome · Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis

ORPHA:1652

Diethylstilbestrol syndrome

DES embryofetopathy · DES syndrome

ORPHA:1916

Digitorenocerebral syndrome

DRC syndrome · Eronen-Somer-Gustafsson syndrome

ORPHA:1674

Distal deletion 3p syndrome

3p- syndrome · Distal monosomy 3p

ORPHA:1620

Double uterus-hemivagina-renal agenesis syndrome

Double uterus and obstructed hemivagina syndrome · OHVIRA syndrome

ORPHA:3411

Ectrodactyly-cleft palate syndrome

ECP syndrome

ORPHA:1889

EEC syndrome

Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome

ORPHA:1896

EEM syndrome

Ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome

ORPHA:1897

Endocrine-cerebro-osteodysplasia syndrome

ECO syndrome

ORPHA:199332

Erythrokeratodermia-cardiomyopathy syndrome

EKC syndrome

ORPHA:476096

Facial dysmorphism-immunodeficiency-livedo-short stature syndrome

FILS syndrome

ORPHA:352712

Febrile infection-related epilepsy syndrome

AERRPS · Acute encephalitis with refractory repetitive partial seizures

ORPHA:163703

Feingold syndrome

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

ORPHA:1305

Focal facial dermal dysplasia type I

Bitemporal aplasia cutis congenita · Brauer syndrome

ORPHA:79133

Fragile X syndrome

FRAXA syndrome · FXS

ORPHA:908

Frey syndrome

Baillarger syndrome · Auriculotemporal syndrome

ORPHA:662240

GAPO syndrome

Growth delay-alopecia-pseudoanodontia-optic atrophy syndrome

ORPHA:2067

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

H syndrome

ORPHA:168569

HARP syndrome

Hypoprebetalipoproteinemia-acanthocytosis-retinitis pigmentosa-pallidal degeneration syndrome

ORPHA:157855

HEC syndrome

Hydrocephalus-endocardial fibroelastosis-cataract syndrome

ORPHA:2119

Hemiconvulsion-hemiplegia-epilepsy syndrome

HHE · HHE syndrome

ORPHA:86908

Hemidystonia-hemiatrophy syndrome

HD-HA syndrome

ORPHA:306741

HNF1B-related autosomal dominant tubulointerstitial kidney disease

Renal cysts and diabetes syndrome · HNF1B-MODY

ORPHA:93111

Hyperinsulinism-hyperammonemia syndrome

HI/HA syndrome

ORPHA:35878

Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

HHH syndrome · ORNT1 deficiency

ORPHA:415

Hypertelorism-microtia-facial clefting syndrome

Bixler-Christian-Gorlin syndrome · HMC syndrome

ORPHA:2213

Hyperzincemia and hypercalprotectinemia

PSTPIP1-associated myeloid-related proteinemia inflammatory syndrome · PAMI syndrome

ORPHA:251523

Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome

HEDH syndrome · ANOTHER syndrome

ORPHA:1882

Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome

4H syndrome

ORPHA:88637

Hypoparathyroidism-sensorineural deafness-renal disease syndrome

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

ORPHA:2237

Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome

HOPP syndrome · Hypotrichosis-osteolysis-periodontitis-palmoplantar hyperkeratosis syndrome

ORPHA:307936

IBIDS syndrome

Tay syndrome · Trichothiodystrophy type E

ORPHA:453