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Summary Literature (0)
MIM:615873 - HELSMOORTEL-VAN DER AA SYNDROME; HVDAS

Xenbase Genes: adnp

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014379 - ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder

Disease Ontology (DO):
DOID:0070058 - Helsmoortel-Van Der Aa Syndrome