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
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