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"

73 matching diseasesClear search ×

Cerebro-oculo-facial-lymphatic syndrome

Fryns-Aftimos syndrome

ORPHA:94084

ABCD syndrome

Albinism-black lock-cell migration disorder of the neurocytes of the gut-sensorineural deafness syndrome · Albinism-black lock-cell migration disorder of the neurocytes of the gut-sensorineural hearing loss syndrome

ORPHA:918

Acropectoral syndrome

ACRP syndrome · Syndactyly-preaxial polydactyly-sternal deformity syndrome

ORPHA:85203

Acropectorovertebral dysplasia

F syndrome

ORPHA:957

ADULT syndrome

Acro-dermato-ungual-lacrimal-tooth syndrome · Pigment anomaly-ectrodactyly-hypodontia syndrome

ORPHA:978

Alopecia-hypogonadism-extrapyramidal syndrome

Devriendt-Legius-Fryns syndrome

ORPHA:1011

Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome

AMME complex · AMME syndrome

ORPHA:86818

ANE syndrome

Alopecia-progressive neurological defect-endocrinopathy syndrome

ORPHA:157954

Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome

AEC syndrome · Hay-Wells syndrome

ORPHA:1071

Anophthalmia plus syndrome

Fryns microphthalmia syndrome · Microphthalmia with facial clefting

ORPHA:1104

Antisynthetase syndrome

AS syndrome · Anti-Jo1 syndrome

ORPHA:81

Apert syndrome

ACS1 · Acrocephalosyndactyly type 1

ORPHA:87

Aplastic anemia-intellectual disability-dwarfism syndrome

AMeD syndrome

ORPHA:611216

Arachnodactyly-intellectual disability-dysmorphism syndrome

De Die-Smulders-Vles-Fryns syndrome

ORPHA:1130

Arthrogryposis-renal dysfunction-cholestasis syndrome

ARC syndrome

ORPHA:2697

Ataxia-pancytopenia syndrome

ATXPC syndrome · SAMD9L-related ataxia-pancytopenia syndrome

ORPHA:2585

Autism spectrum disorder due to AUTS2 deficiency

ASD due to AUTS2 deficiency · AUTS2 syndrome

ORPHA:352490

Autosomal recessive distal osteolysis syndrome

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

ORPHA:2776

Bohring-Opitz syndrome

BOS syndrome · Bohring syndrome

ORPHA:97297

C syndrome

OTCS · Opitz C trigonocephaly

ORPHA:1308

CAMOS syndrome

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

ORPHA:83472

Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome

Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural deafness syndrome · CAPOS syndrome

ORPHA:1171

Costello syndrome

FCS syndrome · Faciocutaneoskeletal syndrome

ORPHA:3071

Dermochondrocorneal dystrophy

François syndrome

ORPHA:79149

Difference of sex development-intellectual disability syndrome

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

ORPHA:2983

Distal limb deficiencies-micrognathia syndrome

10q24 microduplication syndrome · Buttiens-Fryns syndrome

ORPHA:1307

Donnai-Barrow syndrome

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

ORPHA:2143

Evans syndrome

Autoimmune hemolytic anemia and autoimmune thrombocytopenia · Immune pancytopenia

ORPHA:1959

Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome

Friedman-Goodman syndrome · FACES syndrome

ORPHA:1969

Facial dysmorphism-hypertrichosis-epilepsy-intellectual disability/developmental delay-gingival overgrowth syndrome

FHEIG syndrome

ORPHA:598603

Facial dysmorphism-immunodeficiency-livedo-short stature syndrome

FILS syndrome

ORPHA:352712

Facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome

FDLAB syndrome · Facial dysmorphism-lens dislocation-anterior segment abnormalities-nontraumatic conjunctive cysts syndrome

ORPHA:412022

Facial onset sensory and motor neuronopathy

FOSMN syndrome

ORPHA:85162

Familial atypical multiple mole melanoma syndrome

B-K mole syndrome · FAMM-PC syndrome

ORPHA:404560

FATCO syndrome

Hecht-Scott syndrome · Fibular aplasia-tibial campomelia-oligosyndactyly syndrome

ORPHA:2492

Felty syndrome

Splenomegaly-neutropenia-rheumatoid arthritis syndrome

ORPHA:47612

FOXG1 syndrome

FOXG1-related epileptic-dyskinetic encephalopathy

ORPHA:561854

FOXP1 Syndrome

FOXP1-retaled intellectual disability-severe speech delay-mild dysmorphism syndrome

ORPHA:391372

Fragile X syndrome

FRAXA syndrome · FXS

ORPHA:908

Fragile X-associated tremor/ataxia syndrome

FXTAS syndrome

ORPHA:93256

Fraser syndrome

Cryptophthalmos-syndactyly syndrome

ORPHA:2052

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

Fryns-Smeets-Thiry syndrome

ORPHA:2058

Growth deficiency-brachydactyly-dysmorphism syndrome

Frias syndrome

ORPHA:2055