Disease #05996 (FPS (Fontaine progeroid syndrome), OMIM:612289)
Official abbreviation |
FPS |
Name |
Fontaine progeroid syndrome |
OMIM ID |
612289 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SLC25A24 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
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