Anophthalmia-hypothalamo-pituitary insufficiency syndrome
ORPHA:1102Beckwith-Wiedemann syndrome due to 11p15 microdeletion
ORPHA:231127Chromosome Y microdeletion syndrome
ORPHA:1646Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion
ORPHA:261190Contractures-developmental delay-Pierre Robin syndrome
ORPHA:436003Deletion 5q35 syndrome
ORPHA:1627Distal 16p11.2 microdeletion syndrome
ORPHA:261222Distal 17p13.1 microdeletion syndrome
ORPHA:319171Distal 17p13.3 microdeletion syndrome
ORPHA:261257Distal 22q11.2 microdeletion syndrome
ORPHA:261330Distal 22q11.2 microduplication syndrome
ORPHA:261337Distal 7q11.23 microdeletion syndrome
ORPHA:254351Distal 7q11.23 microduplication syndrome
ORPHA:261102Distal 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 3p syndrome
ORPHA:1620Distal deletion 6p syndrome
ORPHA:96125Distal limb deficiencies-micrognathia syndrome
ORPHA:1307DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
ORPHA:268261Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion
ORPHA:284169FOXG1 syndrome due to 14q12 microdeletion
ORPHA:261144Hao-Fountain syndrome due to 16p13.2 microdeletion
ORPHA:500055Homozygous 2p21 microdeletion syndrome
ORPHA:369886Ichthyosis-short stature-brachydactyly-microspherophakia syndrome
ORPHA:363992Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion
ORPHA:254528Kleefstra syndrome due to 9q34 microdeletion
ORPHA:96147Mesomelia-synostoses syndrome
ORPHA:2496Micro syndrome
ORPHA:2510Microduplication Xp11.22p11.23 syndrome
ORPHA:217377Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Mowat-Wilson syndrome due to monosomy 2q22
ORPHA:261537Okihiro syndrome due to 20q13 microdeletion
ORPHA:261638Paternal 20q13.2q13.3 microdeletion syndrome
ORPHA:261304PMP22-RAI1 contiguous gene duplication syndrome
ORPHA:477817Proximal 16p11.2 microdeletion syndrome
ORPHA:261197Proximal 16p11.2 microduplication syndrome
ORPHA:370079Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
ORPHA:353281SATB2-associated syndrome due to a chromosomal rearrangement
ORPHA:251028Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion
ORPHA:314655