auriculocondylar syndrome

E2085589 UNEXPLORED

Auriculocondylar syndrome is a rare genetic craniofacial disorder characterized by malformations of the external ear and lower jaw, often leading to distinctive facial features and sometimes hearing or feeding difficulties.

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All labels observed (1)

Label	Occurrences
auriculocondylar syndrome canonical	1

Referenced by (1)

Full triples — surface form annotated when it differs from this entity's canonical label.

GNAI3 → associatedWith → auriculocondylar syndrome ⓘ

subject linked to: GNAI3 gene (for Gαi3 in humans)