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 ×

Vasquez-Hurst-Sotos syndrome

Hypogonadism-gynecomastia-X-linked intellectual disability syndrome

ORPHA:3423

2q37 microdeletion syndrome

Albright hereditary osteodystrophy type 3 · Albright hereditary osteodystrophy-like syndrome

ORPHA:1001

Allan-Herndon-Dudley syndrome

AHDS · MCT8 deficiency

ORPHA:59

Alopecia-contractures-dwarfism-intellectual disability syndrome

ACD-intellectual disability syndrome

ORPHA:1005

Alopecia-epilepsy-pyorrhea-intellectual disability syndrome

Shokeir syndrome

ORPHA:1008

Alopecia-intellectual disability syndrome

Perniola-Krajewska-Carnevale syndrome

ORPHA:2850

Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome

Devriendt-Vandenberghe-Fryns syndrome

ORPHA:1014

Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16

ATR syndrome linked to chromosome 16 · ATR syndrome, deletion type

ORPHA:98791

Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome

AMME complex · AMME syndrome

ORPHA:86818

Aniridia-cerebellar ataxia-intellectual disability syndrome

Gillespie syndrome

ORPHA:1065

Aniridia-intellectual disability syndrome

Walker-Dyson syndrome

ORPHA:1068

ANK3-related intellectual disability-sleep disturbance syndrome

ORPHA:356996

Anophthalmia-heart and pulmonary anomalies-intellectual disability syndrome

ORPHA:91129

Aplastic anemia-intellectual disability-dwarfism syndrome

AMeD syndrome

ORPHA:611216

Arachnodactyly-intellectual disability-dysmorphism syndrome

De Die-Smulders-Vles-Fryns syndrome

ORPHA:1130

Ataxia-deafness-intellectual disability syndrome

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

ORPHA:1188

Atkin-Flaitz syndrome

X-linked intellectual disability, Atkin type

ORPHA:1193

Birk-Barel syndrome

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

ORPHA:166108

Blepharophimosis-intellectual disability syndrome

ORPHA:293642

Blepharophimosis-intellectual disability syndrome, SBBYS type

SBBYS variant of Ohdo syndrome · Hypothyroidism-dysmorphism-postaxial polydactyly-intellectual disability syndrome

ORPHA:3047

Cataract-hypertrichosis-intellectual disability syndrome

CAHMR syndrome

ORPHA:1375

Cataract-intellectual disability-hypogonadism syndrome

Martsolf syndrome

ORPHA:1387

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

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

Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome

ORPHA:363741

Craniodigital-intellectual disability syndrome

Scott craniodigital syndrome · Scott-Bryant-Graham syndrome

ORPHA:1514

Cryptorchidism-arachnodactyly-intellectual disability syndrome

Van Benthem-Driessen-Hanveld syndrome

ORPHA:1548

Cutis verticis gyrata-intellectual disability syndrome

McDowall syndrome

ORPHA:1557

De Barsy syndrome

Cutis laxa-corneal clouding-intellectual disability syndrome · Progeroid syndrome, De Barsy type

ORPHA:2962

Deafness-intellectual disability syndrome, Martin-Probst type

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

ORPHA:85321

Developmental delay-facial dysmorphism syndrome due to MED13L deficiency

MED13L-related intellectual disability syndrome

ORPHA:369891

Difference of sex development-intellectual disability syndrome

Verloes-Gillerot-Fryns syndrome · Disorder of sex development-intellectual disability syndrome

ORPHA:2983

Digital anomalies-intellectual disability-short stature syndrome

ORPHA:352487

DYRK1A-related intellectual disability syndrome

DYRK1A syndrome

ORPHA:464306

Early-onset parkinsonism-intellectual disability syndrome

Laxova-Opitz syndrome · Waisman syndrome

ORPHA:2379

Fallot complex-intellectual disability-growth delay syndrome

Bindewald-Ulmer-Müller syndrome

ORPHA:3304

GMS syndrome

Goniodysgenesis-intellectual disability-short stature syndrome

ORPHA:2090

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

Growth delay-intellectual disability-hepatopathy syndrome

ORPHA:541423

Hair defect-photosensitivity-intellectual disability syndrome

Calderón-González-Cantu syndrome

ORPHA:1408

Hennekam syndrome

Lymphedema-lymphangiectasia-intellectual disability syndrome

ORPHA:2136

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

Hypogonadism-mitral valve prolapse-intellectual disability syndrome

Cantalamessa-Baldini-Ambrosi syndrome

ORPHA:2233

Hypospadias-intellectual disability, Goldblatt type syndrome

Goldblatt-Wallis syndrome

ORPHA:2261