Disease #03129 (CWS2 (Cowden syndrome, type 2 (CWS-2)), OMIM:612359)
Official abbreviation |
CWS2 |
Name |
Cowden syndrome, type 2 (CWS-2) |
OMIM ID |
612359 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SDHB |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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