DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
ORPHA:268261Emanuel syndrome
ORPHA:96170Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion
ORPHA:284169Facial dysmorphism-Intellectual disability-rhombencephalosynapsis syndrome
ORPHA:693549FOXG1 syndrome due to 14q12 microdeletion
ORPHA:261144Hao-Fountain syndrome due to 16p13.2 microdeletion
ORPHA:500055Ichthyosis-short stature-brachydactyly-microspherophakia syndrome
ORPHA:363992Kleefstra syndrome due to 9q34 microdeletion
ORPHA:96147Lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster
ORPHA:615986Mesomelia-synostoses syndrome
ORPHA:2496Mitochondrial DNA depletion syndrome
ORPHA:35698Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Multiple mitochondrial DNA deletion syndrome
ORPHA:254807Non-distal deletion 10q syndrome
ORPHA:1581Non-distal deletion 12q syndrome
ORPHA:96160Partial autosomal deletion syndrome
ORPHA:98142Partial deletion of chromosome 1 syndrome
ORPHA:261766Partial deletion of chromosome 10 syndrome
ORPHA:261811Partial deletion of chromosome 11 syndrome
ORPHA:261816Partial deletion of chromosome 12 syndrome
ORPHA:282124Partial deletion of chromosome 16 syndrome
ORPHA:261826Partial deletion of chromosome 17 syndrome
ORPHA:261831Partial deletion of chromosome 18 syndrome
ORPHA:261836Partial deletion of chromosome 19 syndrome
ORPHA:261841Partial deletion of chromosome 2 syndrome
ORPHA:261771Partial deletion of chromosome 20 syndrome
ORPHA:261846Partial deletion of chromosome 3 syndrome
ORPHA:261776Partial deletion of chromosome 4 syndrome
ORPHA:261781Partial deletion of chromosome 5 syndrome
ORPHA:261786Partial deletion of chromosome 6 syndrome
ORPHA:261791Partial deletion of chromosome 7 syndrome
ORPHA:261796Partial deletion of chromosome 8 syndrome
ORPHA:261801Partial deletion of chromosome 9 syndrome
ORPHA:261806Partial deletion of chromosome X syndrome
ORPHA:263726Partial deletion of the long arm of chromosome 11 syndrome
ORPHA:262092Partial deletion of the short arm of chromosome 11 syndrome
ORPHA:261947Paternal 20q13.2q13.3 microdeletion syndrome
ORPHA:261304Phelan-McDermid syndrome due to 22q13.3 deletion
ORPHA:662169Potocki-Shaffer syndrome
ORPHA:52022Prader-Willi syndrome due to paternal 15q11q13 deletion
ORPHA:98793SATB2-associated syndrome due to a chromosomal rearrangement
ORPHA:251028Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion
ORPHA:314655Smith-Magenis syndrome
ORPHA:819Temple syndrome due to paternal 14q32.2 microdeletion
ORPHA:254525X-linked Alport syndrome-diffuse leiomyomatosis
ORPHA:1018Xp21 deletion syndrome
ORPHA:261476Xp22.3 microdeletion syndrome
ORPHA:1643