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"

165 matching diseasesClear search ×

Hernández-Aguirre Negrete syndrome

Intellectual disability-epilepsy-bulbous nose syndrome

ORPHA:2139

HIDEA syndrome

Severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome

ORPHA:436141

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

Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome

Passwell-Goodman-Siprkowski syndrome

ORPHA:2278

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-cardiac anomalies-short stature-joint laxity syndrome

Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome due to mutation in PUF60 gene

ORPHA:508498

Intellectual disability-cataracts-calcified pinnae-myopathy syndrome

Primrose syndrome

ORPHA:3042

Intellectual disability-cupped ears syndrome

Snijders Blok-Fisher syndrome

ORPHA:656135

Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome

ORPHA:3044

Intellectual disability-epilepsy-extrapyramidal syndrome

ORPHA:468620

Intellectual disability-facial dysmorphism-hand anomalies syndrome

ORPHA:370010

Intellectual disability-facial dysmorphism-joint hypermobility-hearing loss syndrome

Beck-Fahrner syndrome · TET3-related Beck-Fahrner syndrome

ORPHA:684216

Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome

ORPHA:314575

Intellectual disability-hypotonia-facial dysmorphism-macrocephaly syndrome

KMT5B haploinsufficiency neurodevelopmental disorder

ORPHA:684226

Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome

ORPHA:457365

Intellectual disability-myopathy-short stature-endocrine defect syndrome

Chudley-Rozdilsky syndrome

ORPHA:3068

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-abnormal gait-facial dysmorphism syndrome

Skraban-Deardorff syndrome

ORPHA:513456

Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome

MCAHS type 3 · Multiple congenital anomalies-hypotonia-seizures syndrome type 3

ORPHA:369837

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

Kahrizi syndrome

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

ORPHA:168972

KBG syndrome

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

ORPHA:2332

KDM3B-related intellectual disability-facial dysmorphism-short stature syndrome

Diets-Jongmans Syndrome

ORPHA:633004

Keppen-Lubinsky syndrome

Generalized lipodystrophy-progeroid features-severe intellectual disability syndrome

ORPHA:435628

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

Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome

Berlin syndrome · Ectodermal dysplasia, Berlin type

ORPHA:1816

Lipodystrophy-intellectual disability-deafness syndrome

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

ORPHA:50811

Macrocephaly-intellectual disability-autism syndrome

ORPHA:210548

Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome

Sohval-Soffer syndrome

ORPHA:2234

MAN1B1-CDG

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

ORPHA:397941

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

MEHMO syndrome

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

ORPHA:85282

Metaphyseal acroscyphodysplasia

Bellini syndrome · Intellectual disability-short stature-wedge-shaped epiphyses of knees syndrome

ORPHA:1240

Microcephaly-deafness-intellectual disability syndrome

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

ORPHA:2533

Microcephaly-digital anomalies-intellectual disability syndrome

Kelly-Kirson-Wyatt syndrome

ORPHA:137653

Microcephaly-seizures-intellectual disability-heart disease syndrome

ORPHA:2519

Microcephaly-short stature-intellectual disability-facial dysmorphism syndrome

ORPHA:423306

Mirhosseini-Holmes-Walton syndrome

Pigmentary retinopathy-intellectual disability syndrome

ORPHA:3084

Mowat-Wilson syndrome

Hirschsprung disease-intellectual disability syndrome

ORPHA:2152