Disease #00741 (SGS (Schinzel-Giedion midface retraction syndrome (SGS)), OMIM:269150)
Official abbreviation |
SGS |
Name |
Schinzel-Giedion midface retraction syndrome (SGS) |
OMIM ID |
269150 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
17 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
SETBP1 |
Associated tissues |
- |
Disease features |
autosomal dominant |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|