CK syndrome
ORPHA:251383CLAPO syndrome
ORPHA:168984Classic glucose transporter type 1 deficiency syndrome
ORPHA:71277Classic phenylketonuria
ORPHA:79254Classic stiff person syndrome
ORPHA:443192Classical Ehlers-Danlos syndrome
ORPHA:287CLCN4-related X-linked intellectual disability syndrome
ORPHA:485350Cleft palate-lateral synechia syndrome
ORPHA:2016CLOVES syndrome
ORPHA:140944CNTNAP2-related developmental and epileptic encephalopathy
ORPHA:163681Coats plus syndrome
ORPHA:313838CODAS syndrome
ORPHA:1458COFS syndrome
ORPHA:1466Cogan syndrome
ORPHA:1467Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome
ORPHA:444077Cohen syndrome
ORPHA:193Coloboma-osteopetrosis-microphthalmia-macrocephaly-albinism-deafness syndrome
ORPHA:603494Complement hyperactivation-angiopathic thrombosis-protein-losing enteropathy syndrome
ORPHA:566175Congenital contractural arachnodactyly
ORPHA:115Congenital limbs-face contractures-hypotonia-developmental delay syndrome
ORPHA:562528Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
ORPHA:1875Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Constitutional mismatch repair deficiency syndrome
ORPHA:252202Cooks syndrome
ORPHA:1487Corneodermatoosseous syndrome
ORPHA:3194Corpus callosum agenesis-abnormal genitalia syndrome
ORPHA:2508Costello syndrome
ORPHA:3071Cowden syndrome
ORPHA:201CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199CREST syndrome
ORPHA:90290Curly hair-acral keratoderma-caries syndrome
ORPHA:307766Developmental and epileptic encephalopathy with spike-wave activation in sleep
ORPHA:725Diethylstilbestrol syndrome
ORPHA:1916Digitorenocerebral syndrome
ORPHA:1674Distal deletion 3p syndrome
ORPHA:1620Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Dysequilibrium syndrome
ORPHA:1766Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Facial dysmorphism-shawl scrotum-joint laxity syndrome
ORPHA:1778Fibular aplasia-complex brachydactyly syndrome
ORPHA:2639Glossopalatine ankylosis
ORPHA:141163GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095