Disease #03803 (CHTD2 (heart defects, congenital, nonsyndromic, type 2 (CHTD2), OMIM:614980)
| Official abbreviation |
CHTD2 |
| Name |
heart defects, congenital, nonsyndromic, type 2 (CHTD2 |
| OMIM ID |
614980 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
TAB2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-05-05 07:55:12 +02:00 (CEST) |
Individuals
|