Disease #00271 (SCKL2 (Seckel syndrome, type 2 (SCKL-2)), OMIM:606744)
Official abbreviation |
SCKL2 |
Name |
Seckel syndrome, type 2 (SCKL-2) |
OMIM ID |
606744 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
RBBP8 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-11-22 15:16:48 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|