RGD Annotation Report for DolichocephalyRat Genome Database

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An association has been curated linking SCNM1 and Dolichocephaly in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for human HPO-to-gene-to-disease annotations
223 RGD objects have been annotated to Dolichocephaly (HP:0000268)
0 papers in RGD have been used to annotate SCNM1
Original References(s): MIM:620107

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