Disease #06847 (RTSC2 (Ritscher-Schinzel syndrome 2), OMIM:300963)
Official abbreviation |
RTSC2 |
Name |
Ritscher-Schinzel syndrome 2 |
OMIM ID |
300963 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
CCDC22 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|