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Summary Literature (0)
OMIM:309801 - LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 1; LSDMCA1


Xenbase Genes: hccs, cox7b

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0024552 - linear skin defects with multiple congenital anomalies 1

Disease Ontology (DO):
DOID:0111808 - linear skin defects with multiple congenital anomalies 1
DOID:10629 - microphthalmia