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
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