| C1848794 |
Thyrotropin, Biologically Inactive |
DO |
Meckel syndrome 8
|
0070122 |
| C1848794 |
Thyrotropin, Biologically Inactive |
DO |
congenital nongoitrous hypothyroidism 4
|
0070123 |
| C1848794 |
Thyrotropin, Biologically Inactive |
MONDO |
isolated thyroid-stimulating hormone deficiency
|
0010139 |
| C1848794 |
Thyrotropin, Biologically Inactive |
MONDO |
Meckel syndrome, type 8
|
0013482 |
| C1848794 |
Thyrotropin, Biologically Inactive |
MSH |
Thyrotropin, Biologically Inactive
|
C564765 |
| C1848794 |
Thyrotropin, Biologically Inactive |
OMIM |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4
|
275100 |
| C1848794 |
Thyrotropin, Biologically Inactive |
OMIM |
THYROTROPIN, BIOLOGICALLY INACTIVE
|
275100 |
| C1848794 |
Thyrotropin, Biologically Inactive |
OMIM |
TSH DEFICIENCY
|
275100 |
| C1848794 |
Thyrotropin, Biologically Inactive |
OMIM |
THYROTROPIN DEFICIENCY, ISOLATED
|
275100 |
| C1848794 |
Thyrotropin, Biologically Inactive |
ORDO |
Isolated thyroid-stimulating hormone deficiency
|
90674 |