Diaphyseal medullary stenosis-bone malignancy syndrome
ORPHA:8518221q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384346,XX testicular difference of sex development
ORPHA:39347,XYY syndrome
ORPHA:8Acrofacial dysostosis, Weyers type
ORPHA:952Acropectorovertebral dysplasia
ORPHA:957Acute interstitial pneumonia
ORPHA:79126Aicardi syndrome
ORPHA:50Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818ANE syndrome
ORPHA:157954Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
ORPHA:1071Antiphospholipid syndrome
ORPHA:80Antisynthetase syndrome
ORPHA:81Arthrogryposis-renal dysfunction-cholestasis syndrome
ORPHA:2697Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome
ORPHA:314404Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal recessive spastic paraplegia type 21
ORPHA:101001B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome
ORPHA:567502Ballard syndrome
ORPHA:93395BIDS syndrome
ORPHA:1245Blepharo-cheilo-odontic syndrome
ORPHA:1997Bohring-Opitz syndrome
ORPHA:97297BOR syndrome
ORPHA:107Brachymorphism-onychodysplasia-dysphalangism syndrome
ORPHA:1292Branchioskeletogenital syndrome
ORPHA:1299C syndrome
ORPHA:1308Cancer-associated retinopathy
ORPHA:71505CANDLE syndrome
ORPHA:325004Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Char syndrome
ORPHA:46627CHARGE syndrome
ORPHA:138Childhood disintegrative disorder
ORPHA:168782Chronic atrial and intestinal dysrhythmia syndrome
ORPHA:435988Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383Classic progressive supranuclear palsy syndrome
ORPHA:240071CNTNAP2-related developmental and epileptic encephalopathy
ORPHA:163681Complement hyperactivation-angiopathic thrombosis-protein-losing enteropathy syndrome
ORPHA:566175Congenital contractural arachnodactyly
ORPHA:115Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Corneal dystrophy-perceptive deafness syndrome
ORPHA:1490