RGD Annotation Report for nonsyndromic aplasia cutis congenitaRat Genome Database

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An association has been curated linking BMS1 and nonsyndromic aplasia cutis congenita in Sus scrofa.

The association was inferred from sequence orthology (ISO)
The annotation was made from OMIM Disease Annotation Pipeline
The annotation has been inferred from sequence orthology with BMS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
1 RGD objects have been annotated to nonsyndromic aplasia cutis congenita (DOID:0080661)
0 papers in RGD have been used to annotate BMS1

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.