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"

180 matching diseasesClear search ×

DYRK1A-related intellectual disability syndrome

DYRK1A syndrome

ORPHA:464306

Dysequilibrium syndrome

CAMRQ syndrome · Non-progressive cerebellar ataxia-intellectual disability syndrome

ORPHA:1766

Early-onset epilepsy-intellectual disability-brain anomalies syndrome

Congenital disorder of glycosylation due to PIGG deficiency · PIGG-CDG

ORPHA:488635

Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome

Epilepsy-cortical blindness-intellectual disability-facial dysmorphism syndrome

ORPHA:411986

Early-onset parkinsonism-intellectual disability syndrome

Laxova-Opitz syndrome · Waisman syndrome

ORPHA:2379

Fallot complex-intellectual disability-growth delay syndrome

Bindewald-Ulmer-Müller syndrome

ORPHA:3304

Feingold syndrome

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

ORPHA:1305

Feingold syndrome type 1

Brunner-Winter syndrome type 1 · Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1

ORPHA:391641

Feingold syndrome type 2

Brachydactyly-short stature-microcephaly syndrome · Brunner-Winter syndrome type 2

ORPHA:391646

Female restricted epilepsy with intellectual disability

Juberg-Hellman syndrome · EFMR

ORPHA:101039

Filippi syndrome

Type 1 syndactyly-microcephaly-intellectual disability syndrome

ORPHA:3255

Focal epilepsy-intellectual disability-cerebro-cerebellar malformation

Focal epilepsy-intellectual disability-dysarthria-ataxia syndrome

ORPHA:352587

Growth delay due to insulin-like growth factor type 1 deficiency

Growth delay-hearing loss-intellectual disability syndrome · IGF-1 deficiency

ORPHA:73272

Growth delay-intellectual disability-hepatopathy syndrome

ORPHA:541423

Hair defect-photosensitivity-intellectual disability syndrome

Calderón-González-Cantu syndrome

ORPHA:1408

Hennekam syndrome

Lymphedema-lymphangiectasia-intellectual disability syndrome

ORPHA:2136

Hepatic fibrosis-renal cysts-intellectual disability syndrome

Thompson-Baraitser syndrome

ORPHA:2031

Hernández-Aguirre Negrete syndrome

Intellectual disability-epilepsy-bulbous nose syndrome

ORPHA:2139

HSD10 disease, atypical type

HSD10 deficiency, atypical type · Syndromic X-linked intellectual disability type 10

ORPHA:85295

Hyperphosphatasia-intellectual disability syndrome

Mabry syndrome

ORPHA:247262

Hypogonadism-mitral valve prolapse-intellectual disability syndrome

Cantalamessa-Baldini-Ambrosi syndrome

ORPHA:2233

Hypospadias-intellectual disability, Goldblatt type syndrome

Goldblatt-Wallis syndrome

ORPHA:2261

Infantile neurodegeneration-progressive spasticity-intellectual disability-white matter lesions syndrome

HPDL-related infantile neurodegeneration-progressive spasticity-intellectual disability-white matter lesions syndrome · HPDL-related Leigh-like encephalopathy

ORPHA:641353

Intellectual disability syndrome due to a DYRK1A point mutation

DYRK1A-related intellectual disability syndrome due to a point mutation

ORPHA:464311

Intellectual disability-alacrima-achalasia syndrome

ORPHA:289483

Intellectual disability-brachydactyly-Pierre Robin syndrome

ORPHA:364577

Intellectual disability-cataracts-calcified pinnae-myopathy syndrome

Primrose syndrome

ORPHA:3042

Intellectual disability-cupped ears syndrome

Snijders Blok-Fisher syndrome

ORPHA:656135

Intellectual disability-epilepsy-dental anomalies-facial dysmorphism syndrome

Den Hoed-De Boer-Voisin syndrome

ORPHA:684232

Intellectual disability-epilepsy-extrapyramidal syndrome

ORPHA:468620

Intellectual disability-expressive aphasia-facial dysmorphism syndrome

SETBP1 haploinsufficiency disorder · Intellectual disability-loss of expressive language-facial dysmorphism syndrome

ORPHA:436151

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

MOMES syndrome

ORPHA:397973

Intellectual disability-polydactyly-uncombable hair syndrome

Kozlowski-Krajewska syndrome

ORPHA:3082

Intellectual disability-seizures-macrocephaly-obesity syndrome

Der(8)t(8;12)

ORPHA:369950

Intellectual disability-short stature-hypertelorism syndrome

Stoll-Géraudel-Chauvin syndrome

ORPHA:3074

Intellectual disability-spasticity-ectrodactyly syndrome

Jancar syndrome

ORPHA:1891

Intellectual disability-strabismus syndrome

ORPHA:363528

Intellectual disability, Buenos-Aires type

Mutchinick syndrome

ORPHA:3079

Intellectual disability, Wolff type

Wolff-Zimmermann syndrome

ORPHA:3080

Kahrizi syndrome

Intellectual disability, Kahrizi type · Intellectual disability-cataract-coloboma-kyphosis syndrome

ORPHA:168972

Laryngeal abductor paralysis-intellectual disability syndrome

Plott syndrome

ORPHA:2375

Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome

Late-onset localized JEB-intellectual disability syndrome

ORPHA:231556

Lipodystrophy-intellectual disability-deafness syndrome

Rajab-Spranger syndrome · Lipodystrophy-intellectual disability-hearing loss syndrome

ORPHA:50811

Macrocephaly-intellectual disability-autism syndrome

ORPHA:210548

MAN1B1-CDG

Congenital disorder of glycosylation type 2 due to MAN1B1 deficiency · Congenital disorder of glycosylation type II due to MAN1B1 deficiency

ORPHA:397941

Marfanoid habitus-autosomal recessive intellectual disability syndrome

Fragoso-Cantú syndrome

ORPHA:2463

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

Microcephaly-deafness-intellectual disability syndrome

Kawashima-Tsuji syndrome · Microcephaly-hearing loss-intellectual disability syndrome

ORPHA:2533