Autosomal recessive spastic paraplegia type 23
ORPHA:101003Wolcott-Rallison syndrome
ORPHA:1667Zollinger-Ellison syndrome
ORPHA:91321q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384347,XYY syndrome
ORPHA:8Acrocardiofacial syndrome
ORPHA:2008Acrogeria
ORPHA:2500Acropectorovertebral dysplasia
ORPHA:957Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818ANE syndrome
ORPHA:157954Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
ORPHA:1071Antisynthetase syndrome
ORPHA:81Aplastic anemia-intellectual disability-dwarfism syndrome
ORPHA:611216Arthrogryposis-renal dysfunction-cholestasis syndrome
ORPHA:2697Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Blepharo-cheilo-odontic syndrome
ORPHA:1997Blepharophimosis-intellectual disability syndrome, Ohdo type
ORPHA:2728BNAR syndrome
ORPHA:217266Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
ORPHA:91135Bohring-Opitz syndrome
ORPHA:97297BOR syndrome
ORPHA:107Brachydactyly-elbow wrist dysplasia syndrome
ORPHA:1275Brachymorphism-onychodysplasia-dysphalangism syndrome
ORPHA:1292Branchioskeletogenital syndrome
ORPHA:1299C syndrome
ORPHA:1308CACH syndrome
ORPHA:135Camptodactyly-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:1380Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383Classic progressive supranuclear palsy syndrome
ORPHA:240071CNTNAP2-related developmental and epileptic encephalopathy
ORPHA:163681Congenital contractural arachnodactyly
ORPHA:115Congenital heart defect-round face-developmental delay syndrome
ORPHA:1355Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Corneodermatoosseous syndrome
ORPHA:3194Costello syndrome
ORPHA:3071CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199Crouzon syndrome
ORPHA:207