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"

76 matching diseasesClear search ×

BOR syndrome

Branchiootorenal syndrome · Branchiootorenal spectrum disorder

ORPHA:107

3M syndrome

3-M syndrome · Yakut short stature syndrome

ORPHA:2616

46,XY complete gonadal dysgenesis

46,XY CGD · 46,XY pure gonadal dysgenesis

ORPHA:242

Acropectorovertebral dysplasia

F syndrome

ORPHA:957

Aplasia cutis congenita-intestinal lymphangiectasia syndrome

Bronspiegel-Zelnick syndrome

ORPHA:1116

Apparent mineralocorticoid excess

11-beta-hydroxysteroid dehydrogenase deficiency type 2 · Ulick syndrome

ORPHA:320

Autoimmune polyendocrinopathy type 1

APECED syndrome · APS type 1

ORPHA:3453

Autosomal recessive spastic paraplegia type 21

Mast syndrome · SPG21

ORPHA:101001

Blepharospasm-oromandibular dystonia syndrome

Meige dystonia · Meige syndrome

ORPHA:93964

CK syndrome

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

ORPHA:251383

Costello syndrome

FCS syndrome · Faciocutaneoskeletal syndrome

ORPHA:3071

Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome

Mehes syndrome

ORPHA:3038

Dermochondrocorneal dystrophy

François syndrome

ORPHA:79149

Diaphragmatic defect-limb deficiency-skull defect syndrome

Froster-Huch syndrome

ORPHA:2141

Donnai-Barrow syndrome

DBS/FOAR syndrome · Diaphragmatic hernia-exomphalos-hypertelorism syndrome

ORPHA:2143

Ear-patella-short stature syndrome

Meier-Gorlin syndrome

ORPHA:2554

Facial dysmorphism-immunodeficiency-livedo-short stature syndrome

FILS syndrome

ORPHA:352712

Fechtner syndrome

Alport syndrome with leukocyte inclusions and macrothrombocytopenia

ORPHA:1984

Fibrous dysplasia/McCune-Albright syndrome

Fibrous dysplasia/McCune-Albright spectrum · FD/MAS spectrum

ORPHA:595216

Fowler urethral sphincter dysfunction syndrome

Fowler-Christmas-Chapple syndrome · Fowler syndrome

ORPHA:2795

Fragile X syndrome

FRAXA syndrome · FXS

ORPHA:908

Frank-Ter Haar syndrome

Ter Haar syndrome

ORPHA:137834

Fraser syndrome

Cryptophthalmos-syndactyly syndrome

ORPHA:2052

Fraser-like syndrome

ORPHA:2051

Frasier syndrome

ORPHA:347

FRAXF syndrome

ORPHA:100974

Frey syndrome

Baillarger syndrome · Auriculotemporal syndrome

ORPHA:662240

Fried syndrome

ORPHA:85335

Fryns syndrome

Diaphragmatic hernia-facial dysmorphism-distal limb anomalies syndrome

ORPHA:2059

Growth deficiency-brachydactyly-dysmorphism syndrome

Frias syndrome

ORPHA:2055

Hypoplastic tibiae-postaxial polydactyly syndrome

Werner mesomelic syndrome · Hypoplastic tibia-polydactyly syndrome

ORPHA:3332

Intellectual disability-facial dysmorphism-joint hypermobility-hearing loss syndrome

Beck-Fahrner syndrome · TET3-related Beck-Fahrner syndrome

ORPHA:684216

Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome

MOMES syndrome

ORPHA:397973

Intellectual disability, Buenos-Aires type

Mutchinick syndrome

ORPHA:3079

Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome

KLICK syndrome

ORPHA:281201

Li-Fraumeni syndrome

ORPHA:524

Mammary-digital-nail syndrome

MDN syndrome · Onycho-digito-mammary syndrome

ORPHA:238744

Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome

MDPL syndrome · MDP syndrome

ORPHA:363649

Mandibulofacial dysostosis-microcephaly syndrome

MFDM syndrome · Mandibulofacial dysostosis, Guion-Almeida type

ORPHA:79113

MASA syndrome

Intellectual disability-aphasia-shuffling gait-adducted thumbs syndrome

ORPHA:2466

MASS syndrome

Mitral valve-aorta-skeleton-skin syndrome

ORPHA:99715

Mayer-Rokitansky-Küster-Hauser syndrome

MRKH syndrome · Rokitansky syndrome

ORPHA:3109

Meacham syndrome

Meacham-Winn-Culler syndrome · Rhabdomyomatous dysplasia-cardiopathy-genital anomalies syndrome

ORPHA:3097

Meckel syndrome

Dysencephalia splanchnocystica · Meckel-Gruber syndrome

ORPHA:564

MEDNIK syndrome

Intellectual disability-enteropathy-deafness-peripheral neuropathy-ichthyosis-keratodermia syndrome · Intellectual disability-enteropathy-hearing loss-peripheral neuropathy-ichthyosis-keratodermia syndrome

ORPHA:171851

Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome

MPPH syndrome

ORPHA:83473

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

MEGDEL syndrome

3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome · 3-methylglutaconic aciduria with hearing loss-encephalopathy-Leigh-like syndrome

ORPHA:352328