DYRK1A-related intellectual disability syndrome
ORPHA:46430621q deletion syndrome
ORPHA:5742q13 microdeletion syndrome
ORPHA:6847423C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:2938433q26 microduplication syndrome
ORPHA:9609546,XY complete gonadal dysgenesis
ORPHA:24247,XYY syndrome
ORPHA:8Acrocardiofacial syndrome
ORPHA:2008Acropectorovertebral 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:81Arthrogryposis-renal dysfunction-cholestasis syndrome
ORPHA:2697Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome
ORPHA:314404Autosomal dominant deafness-onychodystrophy syndrome
ORPHA:79499Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Blepharo-cheilo-odontic syndrome
ORPHA:1997BNAR syndrome
ORPHA:217266Bohring-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:1380Celiac artery compression syndrome
ORPHA:293208Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383CNTNAP2-related developmental and epileptic encephalopathy
ORPHA:163681Congenital contractural arachnodactyly
ORPHA:115Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Constitutional mismatch repair deficiency syndrome
ORPHA:252202Contractures-webbed neck-micrognathia-hypoplastic nipples syndrome
ORPHA:314002Corneodermatoosseous 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:307766Deficiency in anterior pituitary function-variable immunodeficiency syndrome
ORPHA:293978DEND syndrome
ORPHA:79134