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Summary Literature (0)
MIM:300887 - LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2

Xenbase Genes: cox7b

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010474 - linear skin defects with multiple congenital anomalies 2
MONDO:0010672 - linear skin defects with multiple congenital anomalies

Disease Ontology (DO):
DOID:0111877 - linear skin defects with multiple congenital anomalies 2