Disease #07005 (NEDGS (neurodevelopmental disorder with poor growth and skeletal anomalies), OMIM:619880)
Official abbreviation |
NEDGS |
Name |
neurodevelopmental disorder with poor growth and skeletal anomalies |
OMIM ID |
619880 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
PCDHGC4 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2023-02-28 12:00:54 +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.
|