parathyroid hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Developmental hypoplasia of the parathyroid gland. (Human Phenotype Ontology, HP_0000860)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003494
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Genes

4 gene mutations causing the parathyroid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ECE1 endothelin converting enzyme 1
GCM2 glial cells missing homolog 2 (Drosophila)
HOXA1 homeobox A1
PHC1 polyhomeotic homolog 1 (Drosophila)