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"

63 matching diseasesClear search ×

Aymé-Gripp syndrome

Brachycephaly-hearing loss-cataract-intellectual disability syndrome · Fine-Lubinsky syndrome

ORPHA:1272

Acropectorovertebral dysplasia

F syndrome

ORPHA:957

ANE syndrome

Alopecia-progressive neurological defect-endocrinopathy syndrome

ORPHA:157954

Autosomal recessive spastic paraplegia type 23

Lison syndrome · SPG23

ORPHA:101003

C syndrome

OTCS · Opitz C trigonocephaly

ORPHA:1308

Cocaine embryofetopathy

Fetal cocaine syndrome

ORPHA:1911

Congenital central hypoventilation syndrome

CCHS · Ondine syndrome

ORPHA:661

Corneodermatoosseous syndrome

CDO syndrome · Stern-Lubinsky-Durrie syndrome

ORPHA:3194

Costello syndrome

FCS syndrome · Faciocutaneoskeletal syndrome

ORPHA:3071

Deafness with labyrinthine aplasia, microtia, and microdontia

Hearing loss with labyrinthine aplasia, microtia, and microdontia · LAMM syndrome

ORPHA:90024

Donnai-Barrow syndrome

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

ORPHA:2143

Duane retraction syndrome

DRS · DURS

ORPHA:233

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

Fetal iodine syndrome

ORPHA:1910

Filippi syndrome

Type 1 syndactyly-microcephaly-intellectual disability syndrome

ORPHA:3255

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

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

H syndrome

ORPHA:168569

Hypergonadotropic hypogonadism-cataract syndrome

Lubinsky syndrome

ORPHA:2410

Inherited epidermodysplasia verruciformis

Lewandowsky-Lutz syndrome · Lutz-Lewandowsky epidermodysplasia verruciformis

ORPHA:302

Jeune syndrome

Asphyxiating thoracic dystrophy of the newborn · JATD

ORPHA:474

Keppen-Lubinsky syndrome

Generalized lipodystrophy-progeroid features-severe intellectual disability syndrome

ORPHA:435628

Kleine-Levin syndrome

ORPHA:33543

L1 syndrome

CRASH syndrome · Corpus callosum hypoplasia-retardation-adducted thumbs-spasticity-hydrocephalus syndrome

ORPHA:275543

Lacrimoauriculodentodigital syndrome

LADD syndrome · LARD syndrome

ORPHA:2363

Laron syndrome

Complete growth hormone insensitivity · GH receptor deficiency

ORPHA:633

Laryngo-onycho-cutaneous syndrome

LOGIC syndrome · Laryngeal and ocular granulation tissue in children from the Indian subcontinent syndrome

ORPHA:2407

Leigh syndrome

Infantile subacute necrotizing encephalopathy · Leigh disease

ORPHA:506

Lelis syndrome

Ectodermal dysplasia-acanthosis nigricans syndrome

ORPHA:140936

Leukoencephalopathy with calcifications and cysts

Labrune syndrome · LCC

ORPHA:542310

LIG4 syndrome

DNA ligase IV deficiency · Ligase 4 syndrome

ORPHA:99812

Limb body wall complex

LBWC syndrome · Body stalk anomaly

ORPHA:2369

Lujan-Fryns syndrome

X-linked intellectual disability with marfanoid habitus

ORPHA:776

LUMBAR syndrome

PELVIS syndrome · Perineal hemangioma-external genitalia malformations-lipomyelomeningocele-vesicorenal abnormalities-imperforate anus-skin tag syndrome

ORPHA:83628