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
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