vertebral body hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, of the main cylindrical portion of the vertebra ventral to the vertebral canal (Mammalian Phenotype Ontology, MP_0004667)
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4 gene mutations causing the vertebral body hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
COL2A1 collagen, type II, alpha 1
NKX3-2 NK3 homeobox 2
PAX1 paired box 1
ROR2 receptor tyrosine kinase-like orphan receptor 2