Disease #05471 (PVNH7 (heterotopia, nodular, periventricular, type 7), OMIM:617201)
| Official abbreviation |
PVNH7 |
| Name |
heterotopia, nodular, periventricular, type 7 |
| OMIM ID |
617201 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NEDD4L |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2018-08-24 17:08:46 +02:00 (CEST) |
| Date last edited |
2024-04-19 19:00:58 +02:00 (CEST) |
Individuals
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