Disease #03996 (PVNH6 (heterotopia, nodular, periventricular, type 6), OMIM:615544)
Official abbreviation |
PVNH6 |
Name |
heterotopia, nodular, periventricular, type 6 |
OMIM ID |
615544 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
C6orf70 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2024-04-19 19:01:53 +02:00 (CEST) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|