Deletion 5q35 syndrome
ORPHA:1627DEND syndrome
ORPHA:79134Dent disease
ORPHA:1652Denys-Drash syndrome
ORPHA:220Diethylstilbestrol syndrome
ORPHA:1916Digitorenocerebral syndrome
ORPHA:1674Dilated cardiomyopathy with ataxia
ORPHA:66634Distal 16p11.2 microdeletion syndrome
ORPHA:261222Distal 17p13.1 microdeletion syndrome
ORPHA:319171Distal 17p13.3 microdeletion syndrome
ORPHA:261257Distal 22q11.2 microdeletion syndrome
ORPHA:261330Distal 7q11.23 microdeletion syndrome
ORPHA:254351Distal deletion 10p syndrome
ORPHA:1580Distal deletion 10q syndrome
ORPHA:96148Distal deletion 12p syndrome
ORPHA:280325Distal deletion 12q syndrome
ORPHA:96149Distal deletion 13q syndrome
ORPHA:1590Distal deletion 14q syndrome
ORPHA:96150Distal deletion 15q syndrome
ORPHA:1596Distal deletion 17q syndrome
ORPHA:1597Distal deletion 19p syndrome
ORPHA:96129Distal deletion 1q syndrome
ORPHA:36367Distal deletion 4q syndrome
ORPHA:96145Distal deletion 6p syndrome
ORPHA:96125Distal deletion 7p syndrome
ORPHA:96126Distal deletion 9p syndrome
ORPHA:1642Distal duplication 3p syndrome
ORPHA:96071DNA2-related mitochondrial DNA deletion syndrome
ORPHA:352470DOORS syndrome
ORPHA:79500Down syndrome
ORPHA:870Drug reaction with eosinophilia and systemic symptoms
ORPHA:139402Duane retraction syndrome
ORPHA:233DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
ORPHA:268261Epilepsy with myoclonic-atonic seizures
ORPHA:1942Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion
ORPHA:284169Febrile infection-related epilepsy syndrome
ORPHA:163703Frey syndrome
ORPHA:662240H syndrome
ORPHA:168569Hao-Fountain syndrome due to 16p13.2 microdeletion
ORPHA:500055Homozygous 2p21 microdeletion syndrome
ORPHA:369886Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Ichthyosis-short stature-brachydactyly-microspherophakia syndrome
ORPHA:363992Jacobsen syndrome
ORPHA:2308Kleefstra syndrome due to 9q34 microdeletion
ORPHA:96147L1 syndrome
ORPHA:275543Laron syndrome
ORPHA:633Lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster
ORPHA:615986Malpuech syndrome
ORPHA:2453