Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383Classic progressive supranuclear palsy syndrome
ORPHA:240071CNTNAP2-related developmental and epileptic encephalopathy
ORPHA:163681Congenital contractural arachnodactyly
ORPHA:115Congenital generalized hypertrichosis, Ambras type
ORPHA:1023Congenital heart defect-round face-developmental delay syndrome
ORPHA:1355Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
ORPHA:1875Congenital 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:85199Crouzon syndrome
ORPHA:207Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Dent 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:3411Down syndrome
ORPHA:870Drug reaction with eosinophilia and systemic symptoms
ORPHA:139402EAST syndrome
ORPHA:199343Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Feingold syndrome
ORPHA:1305Fragile X syndrome
ORPHA:908Frey syndrome
ORPHA:662240GMS syndrome
ORPHA:2090Gordon syndrome
ORPHA:376Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Helsmoortel-Van der Aa syndrome
ORPHA:404448Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Holmes-Adie syndrome
ORPHA:454718Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268