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chromosome 16p12.1 deletion syndrome, 520kb
MONDO:0007631
alpha thalassemia-intellectual disability syndrome type 1
MONDO:0007716
Rubinstein-Taybi syndrome due to CREBBP mutations
MONDO:0008393
autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
MONDO:0010856
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
MONDO:0012519
proximal 16p11.2 microdeletion syndrome
MONDO:0012756