Disease #01766 (CHNG5 (hypothyroidism, congenital, nongoitrous, type 5 (CHNG5)), OMIM:225250)
| Official abbreviation |
CHNG5 |
| Name |
hypothyroidism, congenital, nongoitrous, type 5 (CHNG5) |
| OMIM ID |
225250 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
33 |
| Phenotype entries for this disease |
33 |
| Associated with 1 gene |
NKX2-5 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-03-16 10:45:39 +01:00 (CET) |
Individuals
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