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 ×

Hair defect-photosensitivity-intellectual disability syndrome

Calderón-González-Cantu syndrome

ORPHA:1408

Helsmoortel-Van der Aa syndrome

ADNP-related syndromic intellectual disability-autism spectrum disorder · ADNP-related Helsmoortel-Van der Aa syndrome

ORPHA:404448

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

Hypospadias-intellectual disability, Goldblatt type syndrome

Goldblatt-Wallis syndrome

ORPHA:2261

Hypotrichosis-intellectual disability, Lopes type

Lopes-Marques de Faria syndrome

ORPHA:2266

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-balding-patella luxation-acromicria syndrome

Scholte-Begeer-van Essen syndrome

ORPHA:3041

Intellectual disability-cupped ears syndrome

Snijders Blok-Fisher syndrome

ORPHA:656135

Intellectual disability-epilepsy-extrapyramidal syndrome

ORPHA:468620

Intellectual disability-hyperkinetic movement-truncal ataxia syndrome

ORPHA:369847

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

KDM5C-related syndromic X-linked intellectual disability

ORPHA:85279

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

Lujan-Fryns syndrome

X-linked intellectual disability with marfanoid habitus

ORPHA:776

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

MASA syndrome

Intellectual disability-aphasia-shuffling gait-adducted thumbs syndrome

ORPHA:2466

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

MEHMO syndrome

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

ORPHA:85282

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-thin corpus callosum-intellectual disability syndrome

ORPHA:397951

Mietens syndrome

Intellectual disability, Mietens-Weber type

ORPHA:2557

Mirhosseini-Holmes-Walton syndrome

Pigmentary retinopathy-intellectual disability syndrome

ORPHA:3084

Mowat-Wilson syndrome

Hirschsprung disease-intellectual disability syndrome

ORPHA:2152

Moynahan syndrome

Alopecia-epilepsy-intellectual disability syndrome, Moynahan type

ORPHA:2574

Nicolaides-Baraitser syndrome

Intellectual disability-sparse hair-brachydactyly syndrome

ORPHA:3051

NKAP-related intellectual disability-facial dysmorphism-marfanoid habitus-scoliosis syndrome

X-linked syndromic intellectual developmental disorder, Hackmann-Di Donato type

ORPHA:700325

Non-specific syndromic intellectual disability

Complex neurodevelopmental disorder

ORPHA:528084

Northern epilepsy

Progressive epilepsy-intellectual disability syndrome, Finnish type · CLN8 disease, Northern epilepsy variant

ORPHA:1947

OBSOLETE: Intellectual disability-unusual facies syndrome

OBSOLETE: Morillo Cucci-Passarge syndrome

ORPHA:3043

OBSOLETE: McLain-Dekaban syndrome

OBSOLETE: Intellectual disability-coloboma-slimness syndrome

ORPHA:2474

OBSOLETE: MECP2 duplication syndrome

OBSOLETE: X-linked intellectual disability-hypotonia-recurrent Infections syndrome · OBSOLETE: Lubs-Arena syndrome

ORPHA:85281

OBSOLETE: Syndromic neurometabolic disease with non-X-linked intellectual disability

ORPHA:182073

OBSOLETE: Syndromic neurometabolic disease with X-linked intellectual disability

ORPHA:182076

OBSOLETE: Trichodermal syndrome-intellectual disability syndrome

OBSOLETE: Katsantoni-Papadakou Lagoyanni syndrome

ORPHA:3360