Disease #05256 (STHAG9 (agenesis, tooth, selective, type 9 (STHAG-9)), OMIM:617275)
Official abbreviation |
STHAG9 |
Name |
agenesis, tooth, selective, type 9 (STHAG-9) |
OMIM ID |
617275 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
GREM2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2017-03-31 14:15:27 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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