2p15p16.1 microdeletion syndrome is a recently described syndrome characterized by developmental delay and facial dysmorphism.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
hypotonia-cystinuria syndrome
MONDO:0011669
chromosome 2p12-p11.2 deletion syndrome
MONDO:0013309
chromosome 2p16.3 deletion syndrome
MONDO:0013696
2p21 microdeletion syndrome
MONDO:0015583
2p13.2 microdeletion syndrome
MONDO:0018207