Carnevale syndrome
ORPHA:2998Autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome
ORPHA:314572Brachydactyly-short stature-retinitis pigmentosa syndrome
ORPHA:166035Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome
ORPHA:2235Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome
ORPHA:306504OBSOLETE: Osteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome
ORPHA:2653Posterior column ataxia-retinitis pigmentosa syndrome
ORPHA:88628Primary ciliary dyskinesia-retinitis pigmentosa syndrome
ORPHA:247522X-linked intellectual disability-retinitis pigmentosa syndrome
ORPHA:8533221q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384346,XY complete gonadal dysgenesis
ORPHA:24247,XYY syndrome
ORPHA:8Acropectoral syndrome
ORPHA:85203Acropectorovertebral 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 hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Blepharo-cheilo-odontic syndrome
ORPHA:1997Blepharophimosis-intellectual disability syndrome, Ohdo type
ORPHA:2728BNAR syndrome
ORPHA:217266Bohring-Opitz syndrome
ORPHA:97297BOR syndrome
ORPHA:107Brachymorphism-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:1340Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380CHIME syndrome
ORPHA:3474Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383Congenital central hypoventilation syndrome
ORPHA:661Congenital contractural arachnodactyly
ORPHA:115Congenital 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