| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/613546 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the aromatase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CYP19A1 | cytochrome P450, family 19, subfamily A, polypeptide 1 |
