|
hypothyroidism, congenital, nongoitrous caused by mutation in NKX2-5
|
9154 |
|
|
hypothyroidism, congenital, nongoitrous, 5
|
9154 |
|
|
hypothyroidism, congenital, nongoitrous, 5; CHNG5
|
http://purl.obolibrary.org/obo/MONDO_0009154 |
|
|
hypothyroidism, congenital, nongoitrous, type 5
|
9154 |
|
|
androgen resistance syndrome
|
19154 |
|
|
testicular feminization syndrome
|
19154 |
|
|
Feminisation - testicular
|
19154 |
|
|
androgen insensitivity syndrome; AIS
|
http://purl.obolibrary.org/obo/MONDO_0019154 |
|
|
testicular feminization syndrome (formerly)
|
19154 |
|
