| C3493776 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1 |
DO |
congenital nongoitrous hypothyroidism 5
|
0070125 |
| C3493776 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1 |
DO |
congenital nongoitrous hypothyroidism 1
|
0070126 |
| C3493776 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1 |
MONDO |
hypothyroidism, congenital, nongoitrous
|
0000045 |
| C3493776 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1 |
MONDO |
hypothyroidism, congenital, nongoitrous, 5
|
0009154 |
| C3493776 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1 |
MONDO |
hypothyroidism due to TSH receptor mutations
|
0010142 |
| C3493776 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1 |
MSH |
Hypothyroidism, Congenital, Nongoitrous, 1
|
C576976 |
| C3493776 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1 |
OMIM |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1
|
275200 |
| C3493776 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1 |
ORDO |
Hypothyroidism due to TSH receptor mutations
|
90673 |