(Q56013887)

English

multiple congenital anomalies due to 14q32.2 maternally expressed gene defect

human disease

MCA due to 14q32.2 maternally expressed gene defect

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class of disease

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http://www.orpha.net/ORDO/Orphanet_254519

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Identifiers

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mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

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