uterine cervix hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size of the cervix, usually due to a reduced number of cells (Mammalian Phenotype Ontology, MP_0009227)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009227
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1 gene mutations causing the uterine cervix hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
HOXA13 homeobox A13