primary vitreous hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description overdevelopment or increased size of the primary vitreous, usually due an increased number of cells (Mammalian Phenotype Ontology, MP_0009621)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009621
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Genes

2 gene mutations causing the primary vitreous hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN2A cyclin-dependent kinase inhibitor 2A
TGFB2 transforming growth factor, beta 2