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 |
- |
Date created |
2021-03-18 12:21:09 +08:00 (CST) |
Date last edited |
N/A |
Individuals
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