Disease #00042 (DS (Down Syndrome), OMIM:190685)
Official abbreviation |
DS |
Name |
Down Syndrome |
OMIM ID |
190685 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Isolated Cases (Sporadic) |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
GATA1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2020-12-13 16:06:38 +08:00 (CST) |
Date last edited |
2021-04-05 14:38:17 +08:00 (CST) |
Individuals
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