Aromatase deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Aromatase deficiency disrupts the synthesis of estradiol, resulting in hirsutism of mothers during gestation of an affected child; pseudohermaphroditism and virilization in women; and tall stature, osteoporosis and obesity in men. (Orphanet Rare Disease Ontology, Orphanet_91)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537436
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Genes

1 genes/proteins associated with the disease Aromatase deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1 2.88009