Coxopodopatellar syndrome
ORPHA:1509CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199Curly hair-acral keratoderma-caries syndrome
ORPHA:307766Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
ORPHA:221145Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Dent disease
ORPHA:1652Denys-Drash syndrome
ORPHA:220Diethylstilbestrol 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:870Dysequilibrium syndrome
ORPHA:1766Early-onset parkinsonism-intellectual disability syndrome
ORPHA:2379EAST syndrome
ORPHA:199343Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Eosinophilic fasciitis
ORPHA:3165Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Facial dysmorphism-immunodeficiency-livedo-short stature syndrome
ORPHA:352712Fibular aplasia-complex brachydactyly syndrome
ORPHA:2639Fragile X syndrome
ORPHA:908GAPO syndrome
ORPHA:2067German syndrome
ORPHA:2077GMS syndrome
ORPHA:2090Goodman syndrome
ORPHA:65798Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569HARP syndrome
ORPHA:157855HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hereditary mucoepithelial dysplasia
ORPHA:1839Hinman syndrome
ORPHA:84085Holmes-Adie syndrome
ORPHA:454718Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Ichthyosis follicularis-alopecia-photophobia syndrome
ORPHA:2273Iridocorneal endothelial syndrome
ORPHA:64734IRVAN syndrome
ORPHA:209943