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"

179 matching diseasesClear search ×

Cooper-Jabs syndrome

Aural atresia-multiple congenital anomalies-intellectual disability syndrome

ORPHA:1488

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

Aniridia-cerebellar ataxia-intellectual disability syndrome

Gillespie syndrome

ORPHA:1065

Aniridia-intellectual disability syndrome

Walker-Dyson syndrome

ORPHA:1068

Aniridia-ptosis-intellectual disability-familial obesity syndrome

ORPHA:1067

ANK3-related intellectual disability-sleep disturbance syndrome

ORPHA:356996

Anophthalmia-heart and pulmonary anomalies-intellectual disability syndrome

ORPHA:91129

Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome

ORPHA:1110

Aplastic anemia-intellectual disability-dwarfism syndrome

AMeD syndrome

ORPHA:611216

Ataxia-deafness-intellectual disability syndrome

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

ORPHA:1188

Autosomal dominant non-syndromic intellectual disability

ORPHA:178469

Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome

ORPHA:404481

Autosomal recessive distal osteolysis syndrome

Distal osteolysis-short stature-intellectual disability syndrome · Petit-Fryns syndrome

ORPHA:2776

Autosomal recessive non-syndromic intellectual disability

AR-NSID · NS-ARID

ORPHA:88616

Birk-Barel syndrome

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

ORPHA:166108

Blepharophimosis-intellectual disability syndrome

ORPHA:293642

BPTF-related intellectual disability-facial dysmorphism-skeletal anomalies syndrome

BPTF-related Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies · BPTF-related NEDDFL

ORPHA:686482

CAMOS syndrome

Cerebellar ataxia-intellectual disability-optic atrophy-skin abnormalities syndrome · SCAR5

ORPHA:83472

Cardiocranial syndrome, Pfeiffer type

Craniosynostosis-congenital heart disease-intellectual disability syndrome · Pfeiffer-Singer-Zschiesche syndrome

ORPHA:2872

Cataract-combined malonic and methylmalonic aciduria-intellectual disability syndrome

ZBTB11-related neurodevelopmental disorder

ORPHA:699835

Cataract-hypertrichosis-intellectual disability syndrome

CAHMR syndrome

ORPHA:1375

Cataract-intellectual disability-hypogonadism syndrome

Martsolf syndrome

ORPHA:1387

Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome

CIMDAG syndrome

ORPHA:603448

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

CHIME syndrome

Coloboma-congenital heart disease-ichthyosiform dermatosis-intellectual disability-ear anomalies syndrome · Congenital disorder of glycosylation due to PIGL deficiency

ORPHA:3474

CLCN4-related X-linked intellectual disability syndrome

Raynaud-Claes syndrome

ORPHA:485350

Cleft palate-congenital heart defect-intellectual disability syndrome

ORPHA:652519

Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion

Del(15)(q14) · Monosomy 15q14

ORPHA:261190

Cleft palate-congenital heart defect-intellectual disability syndrome due to MEIS2 mutation

ORPHA:652514

Cloverleaf skull-multiple congenital anomalies syndrome

ORPHA:93267

Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome

ORPHA:363741

Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome

ELOVL4-related neuro ichthyosis · Congenital ichthyosis-intellectual disability-spastic tetraplegia syndrome

ORPHA:352333

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

Congenital muscular dystrophy-cataract-intellectual disability syndrome

INPP5K-related syndrome

ORPHA:662184

Congenital scalp aplasia cutis-enamel hypoplasia-developmental delay-intellectual disability syndrome

FOSL2-related neurodevelopmental disorder

ORPHA:697356

Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome

Graham-Cox syndrome

ORPHA:52055

Craniodigital-intellectual disability syndrome

Scott craniodigital syndrome · Scott-Bryant-Graham syndrome

ORPHA:1514

Craniofacial dysmorphism-skeletal anomalies-intellectual disability syndrome

TMCO1 defect syndrome

ORPHA:228407

Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome

Developmental delay-short stature-dysmorphic features-sparse hair syndrome · Loucks-Innes syndrome

ORPHA:459061

Cryptorchidism-arachnodactyly-intellectual disability syndrome

Van Benthem-Driessen-Hanveld syndrome

ORPHA:1548

Cutis verticis gyrata-intellectual disability syndrome

McDowall syndrome

ORPHA:1557