Disease table of APLASIA CUTIS CONGENITA, NONSYNDROMIC OMIM ID: 107600

Gene-disease associations table

Gene	Associated with APLASIA CUTIS CONGENITA, NONSYNDROMIC in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
BMS1	ClinVar, OMIM, HUMSAVAR	HGNC link	10q11.21	1	107600