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Summary Literature (0)
MIM:612242 - CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME

Xenbase Genes: pten, bmpr1a

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012830 - chromosome 10q23 deletion syndrome
MONDO:0017380 - juvenile polyposis syndrome
MONDO:0019190 - juvenile polyposis of infancy

Disease Ontology (DO):
DOID:0060389 - chromosome 10q23 deletion syndrome