Disease #05272 (MAIS (insensitivity syndrome, androgen, mild (MAIS)))
| Official abbreviation |
MAIS |
| Name |
insensitivity syndrome, androgen, mild (MAIS) |
| OMIM ID |
- |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
27 |
| Phenotype entries for this disease |
27 |
| Associated with 1 gene |
AR |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-05-23 14:30:23 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|