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 ×

Pitt-Rogers-Danks syndrome

Intellectual disability-dysmorphism-intrauterine growth retardation syndrome

ORPHA:98788

POMT1-related limb-girdle muscular dystrophy R11

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

ORPHA:86812

Preaxial polydactyly-colobomata-intellectual disability syndrome

Pfeiffer-Mayer syndrome

ORPHA:2921

Progressive hypotonia-intellectual disability-facial dysmorphism syndrome due to FYVE-defective RBSN

Progressive hypotonia-intellectual disability-facial dysmorphism syndrome due to FYVE-defective Rabenosyn-5

ORPHA:675782

Proximal Xq28 duplication syndrome

MECP2 duplication syndrome · X-linked intellectual disability syndrome, Lubs type

ORPHA:1762

Pseudo-TORCH syndrome type 1

Band like calcification with simplified gyration and polymicrogyria · BLC-PMG

ORPHA:1229

Pseudoprogeria syndrome

Hal-Berg-Rudolph syndrome · Absent eyebrows and eyelashes-intellectual disability syndrome

ORPHA:2985

Pterygium colli-intellectual disability-digital anomalies syndrome

Khalifa-Graham syndrome

ORPHA:2988

PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation

ORPHA:438216

Ramos-Arroyo syndrome

Corneal anesthesia-hearing loss-intellectual disability syndrome · Corneal anesthesia-deafness-intellectual disability syndrome

ORPHA:1051

Rare genetic syndromic intellectual disability

ORPHA:183763

Rare non-syndromic intellectual disability

Rare NSID

ORPHA:101685

Rare syndromic intellectual disability

ORPHA:102369

Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome

IDMDC

ORPHA:280384

Renpenning syndrome

X-linked intellectual disability due to PQBP1 mutations · X-linked intellectual disability, Renpenning type

ORPHA:3242

Richards-Rundle syndrome

Ketoaciduria-intellectual disability-ataxia-deafness syndrome · Ketoaciduria-intellectual disability-ataxia-hearing loss syndrome

ORPHA:1399

Richieri Costa-da Silva syndrome

Myotonia-intellectual disability-skeletal anomalies syndrome

ORPHA:3101

Sanjad-Sakati syndrome

HRD syndrome · Hypoparathyroidism-intellectual disability-dysmorphism syndrome

ORPHA:2323

Seizures-intellectual disability due to hydroxylysinuria syndrome

ORPHA:79156

SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome

ORPHA:597743

Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome

IQSEC2-related syndromic intellectual disability

ORPHA:397933

Short stature-intellectual disability-eye anomalies-cleft lip/palate syndrome

Richieri Costa-Guion Almeida syndrome

ORPHA:2649

Silver-Russell syndrome due to a point mutation

ORPHA:397590

SIN3-related intellectual disability syndrome due to a point mutation

ORPHA:500166

SLC12A2-related developmental delay-intellectual disability-sensorineural deafness syndrome

ORPHA:633014

SMARCA2-related blepharophimosis-intellectual disability syndrome

ORPHA:637013

Spastic paraplegia-epilepsy-intellectual disability syndrome

SPEMR

ORPHA:2816

Spastic paraplegia-glaucoma-intellectual disability syndrome

ORPHA:2818

Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome

Spastic quadriplegia-retinitis pigmentosa-intellectual disability syndrome

ORPHA:3011

STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome

ORPHA:502434

Syndromic X-linked intellectual disability 7

MRXS7 · X-linked intellectual disability, Ahmad type

ORPHA:85274

Tall stature-intellectual disability-renal anomalies syndrome

Thauvin-Robinet-Faivre syndrome

ORPHA:500095

Thumb stiffness-brachydactyly-intellectual disability syndrome

Piussan-Lenaerts-Mathieu syndrome

ORPHA:1078

Trichomegaly-retina pigmentary degeneration-dwarfism syndrome

Oliver-McFarlane syndrome · Long eyelashes-intellectual disability syndrome

ORPHA:3363

Ulna hypoplasia-intellectual disability syndrome

ORPHA:2249

Wilson-Turner syndrome

WTS · X-linked intellectual disability-gynecomastia-obesity syndrome

ORPHA:3459

Witteveen-Kolk syndrome

SIN3A-related intellectual disability syndrome · WITKOS

ORPHA:500163

X-linked alpha-thalassemia-intellectual disability syndrome

ATR-X syndrome

ORPHA:847

X-linked intellectual disability due to GRIA3 mutations

ORPHA:364028

X-linked intellectual disability-acromegaly-hyperactivity syndrome

ORPHA:85327

X-linked intellectual disability-ataxia-apraxia syndrome

ORPHA:85338

X-linked intellectual disability-craniofacioskeletal syndrome

ORPHA:163979

X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome

Prieto-Badia-Mulas syndrome

ORPHA:2958

X-linked intellectual disability-epilepsy syndrome

ORPHA:2076

X-linked intellectual disability-hypotonia-movement disorder syndrome

ORPHA:457260

X-linked intellectual disability-hypotonic face syndrome

ORPHA:73220

X-linked intellectual disability-macrocephaly-macroorchidism syndrome

Johnson syndrome

ORPHA:85320

X-linked intellectual disability-plagiocephaly syndrome

Hyde Forster-McCarthy-Berry syndrome

ORPHA:2898