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Summary Literature (0)
MIM:182230 - SEPTOOPTIC DYSPLASIA

Xenbase Genes: hesx1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008428 - septooptic dysplasia
MONDO:0013099 - combined pituitary hormone deficiencies, genetic form

Disease Ontology (DO):
DOID:0060857 - septooptic dysplasia