Cleft lip/palate-deafness-sacral lipoma syndrome
ORPHA:200321q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384347,XYY syndrome
ORPHA:8Acropectoral syndrome
ORPHA:85203Acropectorovertebral dysplasia
ORPHA:957Aggressive primary cutaneous T-cell lymphoma
ORPHA:178551Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818Andersen-Tawil syndrome
ORPHA:37553ANE 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:2697Ataxia-telangiectasia
ORPHA:100Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal recessive spastic paraplegia type 23
ORPHA:101003Behr syndrome
ORPHA:1239BIDS syndrome
ORPHA:1245Biliary atresia with splenic malformation syndrome
ORPHA:244283Blepharo-cheilo-odontic syndrome
ORPHA:1997Blue rubber bleb nevus
ORPHA:1059Bohring-Opitz syndrome
ORPHA:97297Böök syndrome
ORPHA:1262BOR syndrome
ORPHA:107Brachymorphism-onychodysplasia-dysphalangism syndrome
ORPHA:1292Branchioskeletogenital syndrome
ORPHA:1299C syndrome
ORPHA:1308Campomelia, Cumming type
ORPHA:1318Cancer-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:2978Chudley-Lowry-Hoar syndrome
ORPHA:93971CK syndrome
ORPHA:251383Coffin-Lowry syndrome
ORPHA:192Congenital contractural arachnodactyly
ORPHA:115Congenital long QT syndrome
ORPHA:768Congenital 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:85199