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Summary Literature (0)
MIM:600145 - SACRAL DEFECT WITH ANTERIOR MENINGOCELE

Xenbase Genes: vangl1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010831 - familial caudal dysgenesis
MONDO:0017607 - caudal regression sequence
MONDO:0017850 - sirenomelia