Encephalocraniocutaneous lipomatosis
ORPHA:239621q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384347,XYY syndrome
ORPHA:8Acrofacial dysostosis, Weyers type
ORPHA:952Acropectorovertebral dysplasia
ORPHA:957Acute interstitial pneumonia
ORPHA:79126Alopecia antibody deficiency
ORPHA:1006Alport 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 hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome
ORPHA:567502Blepharo-cheilo-odontic syndrome
ORPHA:1997Bohring-Opitz syndrome
ORPHA:97297BOR syndrome
ORPHA:107Brachydactyly-nystagmus-cerebellar ataxia syndrome
ORPHA:1246Brachymorphism-onychodysplasia-dysphalangism syndrome
ORPHA:1292Branchioskeletogenital syndrome
ORPHA:1299C syndrome
ORPHA:1308Cancer-associated retinopathy
ORPHA:71505CANDLE syndrome
ORPHA:325004CANOMAD syndrome
ORPHA:71279Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380CHAND syndrome
ORPHA:1401CHARGE syndrome
ORPHA:138Childhood disintegrative disorder
ORPHA:168782Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383Congenital contractural arachnodactyly
ORPHA:115Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Corneal dystrophy-perceptive deafness syndrome
ORPHA:1490Corneodermatoosseous syndrome
ORPHA:3194Costello syndrome
ORPHA:3071CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome
ORPHA:171839Curly hair-acral keratoderma-caries syndrome
ORPHA:307766De Hauwere syndrome
ORPHA:1831