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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
/
Hereditary disease
/
Frontonasal dysplasia
Oculoauriculofrontonasal syndrome
rare
Identifiers
MONDO:0011082
OMIM:601452
Orphanet:398156
Part of
Frontonasal dysplasia
Also known as
OAFNS
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