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"

71 matching diseasesClear search ×

Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome

Aphonia-hearing loss-retinal dystrophy-duplicated halluces-intellectual disability syndrome · Aphonia-deafness-retinal dystrophy-duplicated halluces-intellectual disability syndrome

ORPHA:324540

ADNP-related blepharophimosis-intellectual disability syndrome

ORPHA:700160

Allan-Herndon-Dudley syndrome

AHDS · MCT8 deficiency

ORPHA:59

Alopecia-contractures-dwarfism-intellectual disability syndrome

ACD-intellectual disability syndrome

ORPHA:1005

Alopecia-intellectual disability syndrome

Perniola-Krajewska-Carnevale syndrome

ORPHA:2850

Aniridia-intellectual disability syndrome

Walker-Dyson syndrome

ORPHA:1068

ANK3-related intellectual disability-sleep disturbance syndrome

ORPHA:356996

Ataxia-deafness-intellectual disability syndrome

Reardon-Baraitser syndrome · Ataxia-hearing loss-intellectual disability syndrome

ORPHA:1188

Aymé-Gripp syndrome

Brachycephaly-hearing loss-cataract-intellectual disability syndrome · Fine-Lubinsky syndrome

ORPHA:1272

Birk-Barel syndrome

Intellectual disability-hypotonia-facial dysmorphism syndrome · Birk-Barel Intellectual Disability-Dimorphism syndrome

ORPHA:166108

Blepharophimosis-intellectual disability syndrome

ORPHA:293642

Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome

Hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibers · Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome

ORPHA:90103

CLCN4-related X-linked intellectual disability syndrome

Raynaud-Claes syndrome

ORPHA:485350

Congenital muscular dystrophy-cataract-intellectual disability syndrome

INPP5K-related syndrome

ORPHA:662184

Deafness-intellectual disability syndrome, Martin-Probst type

X-linked hearing loss-intellectual disability syndrome · Martin-Probst syndrome

ORPHA:85321

Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome

Dentinogenesis imperfecta-short stature-deafness-intellectual disability syndrome

ORPHA:71267

Developmental delay-facial dysmorphism syndrome due to MED13L deficiency

MED13L-related intellectual disability syndrome

ORPHA:369891

DOORS syndrome

Deafness-onychodystrophy-osteodystrophy-intellectual disability-seizures syndrome · Autosomal recessive deafness-onychodystrophy syndrome

ORPHA:79500

DYRK1A-related intellectual disability syndrome

DYRK1A syndrome

ORPHA:464306

EAST syndrome

Epilepsy-ataxia-sensorineural hearing loss-tubulopathy syndrome · SeSAME syndrome

ORPHA:199343

GNB5-related intellectual disability-cardiac arrhythmia syndrome

ORPHA:542306

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

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

ORPHA:73272

Hair defect-photosensitivity-intellectual disability syndrome

Calderón-González-Cantu syndrome

ORPHA:1408

Hepatic fibrosis-renal cysts-intellectual disability syndrome

Thompson-Baraitser syndrome

ORPHA:2031

Hyperphosphatasia-intellectual disability syndrome

Mabry syndrome

ORPHA:247262

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-cupped ears syndrome

Snijders Blok-Fisher syndrome

ORPHA:656135

Intellectual disability-expressive aphasia-facial dysmorphism syndrome

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

ORPHA:436151

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-strabismus syndrome

ORPHA:363528

Lambert syndrome

Branchial dysplasia-intellectual disability-inguinal hernia syndrome

ORPHA:1296

Lipodystrophy-intellectual disability-deafness syndrome

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

ORPHA:50811

Marfanoid habitus-autosomal recessive intellectual disability syndrome

Fragoso-Cantú syndrome

ORPHA:2463

Mesomelic dysplasia-digital anomalies-intellectual disability syndrome

ORPHA:632603

Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome

Metaphyseal dysostosis-intellectual disability-conductive hearing loss syndrome

ORPHA:2502

Microcephaly-deafness-intellectual disability syndrome

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

ORPHA:2533

Microcephaly-hearing loss-facial dysmorphism-intellectual disability syndrome

Nabais Sa-de Vries type 1 syndrome · Microcephaly-deafness-facial dysmorphism-intellectual disability syndrome

ORPHA:662179

Mirhosseini-Holmes-Walton syndrome

Pigmentary retinopathy-intellectual disability syndrome

ORPHA:3084

MORM syndrome

Intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome

ORPHA:75858

Myhre syndrome

Myhre-Laryngotracheal stenosis-arthropathy-prognathism-short stature syndrome · Facial dysmorphism-intellectual disability-short stature-hearing loss syndrome

ORPHA:2588

OBSOLETE: Osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome

OBSOLETE: Osteopenia-myopia-deafness-intellectual disability-facial dysmorphism syndrome

ORPHA:91133

Optic atrophy-intellectual disability syndrome

BBSOAS · Bosch-Boonstra-Schaaf optic atrophy syndrome

ORPHA:401777

Osteopenia-intellectual disability-sparse hair syndrome

Kaler-Garrity-Stern syndrome

ORPHA:2324

Partington syndrome

Partington-Mulley syndrome · X-linked intellectual disability-dystonia-dysarthria syndrome

ORPHA:94083

Pinsky-Di George-Harley syndrome

Microphthalmia-intellectual disability syndrome

ORPHA:2895

POMT1-related limb-girdle muscular dystrophy R11

Autosomal recessive limb-girdle muscular dystrophy type 2K · POMT1-related LGMD R11

ORPHA:86812