Gonadal Dysgenesis Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A hypogonadism that is characterized by a progressive loss of germ cells on the developing gonads of an embryo. (Human Disease Ontology, DOID_14447)
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Genes

4 genes associated with the Gonadal Dysgenesis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
BMP7 bone morphogenetic protein 7
INSL3 insulin-like 3 (Leydig cell)
TGFBR3 transforming growth factor, beta receptor III
TSPYL1 TSPY-like 1