Branchioskeletogenital syndrome
ORPHA:1299C syndrome
ORPHA:1308Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
ORPHA:2848Cancer-associated retinopathy
ORPHA:71505CANOMAD syndrome
ORPHA:71279Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Childhood disintegrative disorder
ORPHA:168782Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383Congenital contractural arachnodactyly
ORPHA:115Congenital generalized hypertrichosis, Ambras type
ORPHA:1023Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Corneodermatoosseous syndrome
ORPHA:3194Corpus callosum agenesis-neuronopathy syndrome
ORPHA:1496Costello syndrome
ORPHA:3071CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199Cutis verticis gyrata-thyroid aplasia-intellectual disability syndrome
ORPHA:79482Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Deafness-enamel hypoplasia-nail defects syndrome
ORPHA:3220Dent disease
ORPHA:1652Diethylstilbestrol syndrome
ORPHA:1916Digitorenocerebral syndrome
ORPHA:1674Distal deletion 3p syndrome
ORPHA:1620Donnai-Barrow syndrome
ORPHA:2143DOORS syndrome
ORPHA:79500Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Feingold syndrome
ORPHA:1305Focal facial dermal dysplasia type I
ORPHA:79133Fowler urethral sphincter dysfunction syndrome
ORPHA:2795Fragile X syndrome
ORPHA:908Fraser syndrome
ORPHA:2052Frasier syndrome
ORPHA:347Gardner syndrome
ORPHA:79665GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095Guttmacher syndrome
ORPHA:2957H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Heiner syndrome
ORPHA:99932