C3665349 |
Secondary hypothyroidism |
DO |
Meckel syndrome 8
|
0070122 |
C3665349 |
Secondary hypothyroidism |
DO |
congenital nongoitrous hypothyroidism 4
|
0070123 |
C3665349 |
Secondary hypothyroidism |
HPO |
Secondary hypothyroidism
|
HP:0008245 |
C3665349 |
Secondary hypothyroidism |
HPO |
TSH deficient hypothyroidism
|
HP:0008245 |
C3665349 |
Secondary hypothyroidism |
HPO |
Thyrotropin deficiency
|
HP:0008245 |
C3665349 |
Secondary hypothyroidism |
HPO |
Thyroid stimulating hormone deficiency
|
HP:0008245 |
C3665349 |
Secondary hypothyroidism |
HPO |
Pituitary hypothyroidism
|
HP:0008245 |
C3665349 |
Secondary hypothyroidism |
MONDO |
isolated thyroid-stimulating hormone deficiency
|
0010139 |
C3665349 |
Secondary hypothyroidism |
MONDO |
Meckel syndrome, type 8
|
0013482 |
C3665349 |
Secondary hypothyroidism |
MONDO |
central congenital hypothyroidism
|
0016410 |
C3665349 |
Secondary hypothyroidism |
MSH |
Hypothyroidism
|
D007037 |
C3665349 |
Secondary hypothyroidism |
MSH |
Hypothyroidism, Central
|
D007037 |
C3665349 |
Secondary hypothyroidism |
MSH |
TSH Deficiency
|
D007037 |
C3665349 |
Secondary hypothyroidism |
MSH |
Primary Hypothyroidism
|
D007037 |
C3665349 |
Secondary hypothyroidism |
NCI |
Pituitary Hypothyroidism
|
C121743 |
C3665349 |
Secondary hypothyroidism |
OMIM |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4
|
275100 |
C3665349 |
Secondary hypothyroidism |
OMIM |
THYROTROPIN, BIOLOGICALLY INACTIVE
|
275100 |
C3665349 |
Secondary hypothyroidism |
OMIM |
TSH DEFICIENCY
|
275100 |
C3665349 |
Secondary hypothyroidism |
OMIM |
THYROTROPIN DEFICIENCY, ISOLATED
|
275100 |
C3665349 |
Secondary hypothyroidism |
ORDO |
Central congenital hypothyroidism
|
226298 |
C3665349 |
Secondary hypothyroidism |
ORDO |
Isolated thyroid-stimulating hormone deficiency
|
90674 |