Disease #03857 (FASPS2 (sleep phase syndrome, advanced, familial, type 2 (FASPS2)), OMIM:615224)
| Official abbreviation |
FASPS2 |
| Name |
sleep phase syndrome, advanced, familial, type 2 (FASPS2) |
| OMIM ID |
615224 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CSNK1D |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2019-11-04 08:53:06 +01:00 (CET) |
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