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"

100 matching diseasesClear search ×

Lujan-Fryns syndrome

X-linked intellectual disability with marfanoid habitus

ORPHA:776

Allan-Herndon-Dudley syndrome

AHDS · MCT8 deficiency

ORPHA:59

Alopecia-contractures-dwarfism-intellectual disability syndrome

ACD-intellectual disability syndrome

ORPHA:1005

Atkin-Flaitz syndrome

X-linked intellectual disability, Atkin type

ORPHA:1193

CK syndrome

X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome

ORPHA:251383

CLCN4-related X-linked intellectual disability syndrome

Raynaud-Claes syndrome

ORPHA:485350

Congenital insensitivity to pain with severe intellectual disability

Congenital absence of pain with severe intellectual disability · Congenital analgesia with severe intellectual disability

ORPHA:453510

Congenital muscular dystrophy with intellectual disability

CMD with intellectual disability · CMD-MR

ORPHA:370968

Congenital muscular dystrophy with intellectual disability and severe epilepsy

CDG syndrome type Iu · CDG-Iu

ORPHA:329178

Congenital muscular dystrophy without intellectual disability

Congenital muscular dystrophy-dystroglycanopathy without intellectual disability · CMD without intellectual disability

ORPHA:370980

Deafness-intellectual disability syndrome, Martin-Probst type

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

ORPHA:85321

EGF-related primary hypomagnesemia with intellectual disability

ORPHA:620368

Female restricted epilepsy with intellectual disability

Juberg-Hellman syndrome · EFMR

ORPHA:101039

FRAXE intellectual disability

Intellectual disability associated with fragile site FRAXE

ORPHA:100973

HSD10 disease, atypical type

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

ORPHA:85295

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

Marfanoid habitus-autosomal recessive intellectual disability syndrome

Fragoso-Cantú syndrome

ORPHA:2463

Mietens syndrome

Intellectual disability, Mietens-Weber type

ORPHA:2557

Multiple congenital anomalies/dysmorphic syndrome without intellectual disability

MCA without intellectual disability · Multiple congenital anomalies without intellectual disability with or without dysmorphism

ORPHA:102285

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

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

ORPHA:700325

OBSOLETE: MECP2 duplication syndrome

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

ORPHA:85281

OBSOLETE: Non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature

OBSOLETE: Non-X-linked CDG with intellectual disability as a major feature

ORPHA:371064

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

ORPHA:182073

OBSOLETE: Syndromic neurometabolic disease with X-linked intellectual disability

ORPHA:182076

OBSOLETE: X-linked congenital disorder of glycosylation with intellectual disability as a major feature

OBSOLETE: X-linked CDG with intellectual disability as a major feature

ORPHA:371054

OBSOLETE: X-linked dominant intellectual disability-epilepsy syndrome

ORPHA:93951

OBSOLETE: X-linked intellectual disability-obesity-short stature syndrome

ORPHA:85331

OBSOLETE: X-linked intellectual disability-precocious puberty-obesity syndrome

ORPHA:85318

OBSOLETE: X-linked intellectual disability, Martinez type

ORPHA:775

OBSOLETE: X-linked intellectual disability, Raynaud type

ORPHA:3061

OBSOLETE: X-linked intellectual disability, Schutz type

ORPHA:3062

OBSOLETE: X-linked intellectual disability, Wittner type

ORPHA:3064

Partington syndrome

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

ORPHA:94083

Proximal Xq28 duplication syndrome

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

ORPHA:1762

Rare genetic intellectual disability

ORPHA:183757

Rare intellectual disability

ORPHA:87277

Renpenning syndrome

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

ORPHA:3242

Severe X-linked intellectual disability, Gustavson type

Gustavson syndrome

ORPHA:3078

Syndromic X-linked intellectual disability 7

MRXS7 · X-linked intellectual disability, Ahmad type

ORPHA:85274

Vasquez-Hurst-Sotos syndrome

Hypogonadism-gynecomastia-X-linked intellectual disability syndrome

ORPHA:3423

Wilson-Turner syndrome

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

ORPHA:3459

X-linked alpha-thalassemia-intellectual disability syndrome

ATR-X syndrome

ORPHA:847

X-linked cerebral-cerebellar-coloboma syndrome

X-linked intellectual disability, Kroes type

ORPHA:163961

X-linked intellectual disability due to GRIA3 mutations

ORPHA:364028

X-linked intellectual disability with isolated growth hormone deficiency

MRGH

ORPHA:67045

X-linked intellectual disability-acromegaly-hyperactivity syndrome

ORPHA:85327