Eosinophilic fasciitis
ORPHA:316521q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384346,XY complete gonadal dysgenesis
ORPHA:24247,XYY syndrome
ORPHA:8Acrocardiofacial syndrome
ORPHA:2008Acropectorovertebral dysplasia
ORPHA:957Alopecia-epilepsy-pyorrhea-intellectual disability syndrome
ORPHA:1008Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818ANE syndrome
ORPHA:157954Angelman syndrome
ORPHA:72Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
ORPHA:1071Antisynthetase syndrome
ORPHA:81Aplastic anemia-intellectual disability-dwarfism syndrome
ORPHA:611216Arthrogryposis-renal dysfunction-cholestasis syndrome
ORPHA:2697Asherman syndrome
ORPHA:137686Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal dominant intellectual disability-craniofacial dysmorphism-macrocephaly-hypotonia syndrome due to H1-4 mutation
ORPHA:642763B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome
ORPHA:567502Blepharo-cheilo-odontic syndrome
ORPHA:1997Blue rubber bleb nevus
ORPHA:1059Bohring-Opitz syndrome
ORPHA:97297BOR syndrome
ORPHA:107Brachymorphism-onychodysplasia-dysphalangism syndrome
ORPHA:1292Branchioskeletogenital syndrome
ORPHA:1299C syndrome
ORPHA:1308Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
ORPHA:2848Cancer-associated retinopathy
ORPHA:71505Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380CHAND syndrome
ORPHA:1401Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383CNTNAP2-related developmental and epileptic encephalopathy
ORPHA:163681Cogan syndrome
ORPHA:1467Congenital contractural arachnodactyly
ORPHA:115Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Congenital thrombotic thrombocytopenic purpura
ORPHA:93583Corneodermatoosseous syndrome
ORPHA:3194Costello syndrome
ORPHA:3071CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199Curly hair-acral keratoderma-caries syndrome
ORPHA:307766