Disease #05983 (TPFS (Turnpenny-Fry syndrome (TPFS)), OMIM:618371)
| Official abbreviation |
TPFS |
| Name |
Turnpenny-Fry syndrome (TPFS) |
| OMIM ID |
618371 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PCGF2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-10-28 11:14:55 +02:00 (CEST) |
| Date last edited |
N/A |
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