Label | Id |
---|
CHNG5 | 0009154 | |
NKX2-5 hypothyroidism, congenital, nongoitrous | 0009154 | |
hypothyroidism, congenital, nongoitrous caused by mutation in NKX2-5 | 0009154 | |
hypothyroidism, congenital nongoitrous, 5 | 0009154 | |
hypothyroidism, congenital, nongoitrous, 5 | 0009154 | |
hypothyroidism, congenital, nongoitrous, type 5 | 0009154 |