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) |
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