Disease #00730 (SYNS1 (synostoses, multiple syndrome, type 1 (SYNS1)), OMIM:186500)
Official abbreviation |
SYNS1 |
Name |
synostoses, multiple syndrome, type 1 (SYNS1) |
OMIM ID |
186500 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
12 |
Phenotype entries for this disease |
12 |
Associated with 1 gene |
NOG |
Associated tissues |
- |
Disease features |
- |
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
|