Disease #05268 (SCKL1 (Seckel syndrome, type 1), OMIM:210600)
| Official abbreviation |
SCKL1 |
| Name |
Seckel syndrome, type 1 |
| OMIM ID |
210600 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
5 |
| Associated with 1 gene |
ATR |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-05-18 15:07:04 +02:00 (CEST) |
| Date last edited |
2023-03-14 15:38:48 +01:00 (CET) |
Individuals
|