Dent disease
ORPHA:1652Denys-Drash syndrome
ORPHA:220Desbuquois syndrome
ORPHA:1425Developmental and epileptic encephalopathy with spike-wave activation in sleep
ORPHA:725Diethylstilbestrol syndrome
ORPHA:1916Digitorenocerebral syndrome
ORPHA:1674Dilated cardiomyopathy with ataxia
ORPHA:66634Distal deletion 3p syndrome
ORPHA:1620Dobrow syndrome
ORPHA:3262DOORS syndrome
ORPHA:79500Down syndrome
ORPHA:870Dravet syndrome
ORPHA:33069Drug reaction with eosinophilia and systemic symptoms
ORPHA:139402Duane retraction syndrome
ORPHA:233Duplication of the pituitary gland
ORPHA:314621Dursun syndrome
ORPHA:178503DYRK1A-related intellectual disability syndrome
ORPHA:464306Epilepsy with myoclonic-atonic seizures
ORPHA:1942Epiphyseal dysplasia-hearing loss-dysmorphism syndrome
ORPHA:1825Febrile infection-related epilepsy syndrome
ORPHA:163703Fibular aplasia-complex brachydactyly syndrome
ORPHA:2639Frey syndrome
ORPHA:662240Generalized resistance to thyroid hormone
ORPHA:3221Gingival fibromatosis-progressive deafness syndrome
ORPHA:2027Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome
ORPHA:2084H syndrome
ORPHA:168569HIDEA syndrome
ORPHA:436141High myopia-sensorineural deafness syndrome
ORPHA:363396Hirschsprung disease-deafness-polydactyly syndrome
ORPHA:2155Hyperzincemia and hypercalprotectinemia
ORPHA:251523Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypotrichosis-deafness syndrome
ORPHA:330029Jervell and Lange-Nielsen syndrome
ORPHA:90647Johnson neuroectodermal syndrome
ORPHA:2316Keratoderma hereditarium mutilans
ORPHA:494L1 syndrome
ORPHA:275543Laryngeal abductor paralysis-intellectual disability syndrome
ORPHA:2375LUMBAR syndrome
ORPHA:83628MASS syndrome
ORPHA:99715Matthew-Wood syndrome
ORPHA:2470Mohr-Tranebjaerg syndrome
ORPHA:52368Monosomy 9p syndrome
ORPHA:261112Multiple endocrine neoplasia type 2A
ORPHA:247698Multiple synostoses syndrome
ORPHA:3237Musculocontractural Ehlers-Danlos syndrome
ORPHA:2953Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
ORPHA:86841Myoclonus-cerebellar ataxia-deafness syndrome
ORPHA:2589N syndrome
ORPHA:2608