Disease #00089 (CH (Congenital hypothyroidism))
Official abbreviation |
CH |
Name |
Congenital hypothyroidism |
OMIM ID |
- |
Inheritance |
- |
Individuals reported having this disease |
20 |
Phenotype entries for this disease |
2 |
Associated with 3 genes |
FOXE1, TPO, TSHR |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|