Term: Aplasia Cutis Congenita, Reticulolinear, with Microcephaly, Facial Dysmorphism, and Other Congenital Anomalies; APLCC
OMIM ID: 300887

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene	Human Gene		Characteristics of this human disease are associated with mutations in...
Cox7b COX7B			...the human gene.      MGI data currently do not associate this disease with mutations in the orthologous mouse gene.