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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
/
Hereditary disease
/
Ear malformation
/
Auriculocondylar syndrome
Question mark ears, isolated
rare
Identifiers
MONDO:0013013
OMIM:612798
Causal genes
EDN1
Part of
Auriculocondylar syndrome
Also known as
QME
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