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"

123 matching diseasesClear search ×

Urofacial syndrome

Hydronephrosis-inverted smile syndrome · Ochoa syndrome

ORPHA:2704

22q11.2 deletion syndrome

22q11DS · CATCH 22

ORPHA:567

3C syndrome

Craniocerebellocardiac dysplasia · Ritscher-Schinzel syndrome

ORPHA:7

3M syndrome

3-M syndrome · Yakut short stature syndrome

ORPHA:2616

8q22.1 microdeletion syndrome

Monosomy 8q22.1 · Nablus mask-like facial syndrome

ORPHA:178303

Aarskog-Scott syndrome

Aarskog syndrome · Faciodigitogenital syndrome

ORPHA:915

Acrocardiofacial syndrome

ACFS · CCGE syndrome

ORPHA:2008

Acromegaloid facial appearance syndrome

ORPHA:965

Acropectorovertebral dysplasia

F syndrome

ORPHA:957

Antisynthetase syndrome

AS syndrome · Anti-Jo1 syndrome

ORPHA:81

Autism-facial port-wine stain syndrome

ORPHA:137911

Autosomal dominant popliteal pterygium syndrome

Facio-genito-popliteal syndrome · Popliteal web syndrome

ORPHA:1300

Blepharophimosis-intellectual disability syndrome, Ohdo type

BMRS, Ohdo type · Blepharophimosis syndrome, Ohdo type

ORPHA:2728

Branchio-oculo-facial syndrome

BOFS

ORPHA:1297

C syndrome

OTCS · Opitz C trigonocephaly

ORPHA:1308

Cardiospondylocarpofacial syndrome

Forney-Robinson-Pascoe syndrome · Mitral regurgitation-deafness-skeletal anomalies syndrome

ORPHA:3238

Carnevale syndrome

3MC2 syndrome · Carnevale-Krajewska-Fischetto syndrome

ORPHA:2998

Cataract-nephropathy-encephalopathy syndrome

Crome syndrome

ORPHA:1380

Cerebellar-facial-dental syndrome

Cerebellofaciodental syndrome

ORPHA:444072

Cerebro-oculo-facial-lymphatic syndrome

Fryns-Aftimos syndrome

ORPHA:94084

CK syndrome

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

ORPHA:251383

Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome

CHOPS syndrome

ORPHA:444077

Congenital central hypoventilation syndrome

CCHS · Ondine syndrome

ORPHA:661

Costello syndrome

FCS syndrome · Faciocutaneoskeletal syndrome

ORPHA:3071

Deafness-craniofacial syndrome

Hearing loss-craniofacial syndrome

ORPHA:3241

Distal deletion 3p syndrome

3p- syndrome · Distal monosomy 3p

ORPHA:1620

Donnai-Barrow syndrome

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

ORPHA:2143

Double uterus-hemivagina-renal agenesis syndrome

Double uterus and obstructed hemivagina syndrome · OHVIRA syndrome

ORPHA:3411

Ehlers-Danlos/osteogenesis imperfecta syndrome

EDS/OI syndrome

ORPHA:230857

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

Faciocardiorenal syndrome

Eastman-Bixler syndrome

ORPHA:1973

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

Feingold syndrome

Brunner-Winter syndrome · Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum

ORPHA:1305

Felty syndrome

Splenomegaly-neutropenia-rheumatoid arthritis syndrome

ORPHA:47612

Femoral-facial syndrome

FFS · FHUFS

ORPHA:1988

Fibrous dysplasia/McCune-Albright syndrome

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

ORPHA:595216

Flat face-microstomia-ear anomaly syndrome

Blepharophimosis-telecanthus-microstomia syndrome · Simosa-Penchaszadeh-Bustos syndrome

ORPHA:1968

FLOTCH syndrome

Leukonychia totalis-trichilemmal cysts-ciliary dystrophy syndrome

ORPHA:2045

Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome

FHONDA syndrome

ORPHA:397618

Fowler urethral sphincter dysfunction syndrome

Fowler-Christmas-Chapple syndrome · Fowler syndrome

ORPHA:2795

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