Disease #04367 (PHPVAR (vitreous, primary, hyperplastic, persistent, autosomal recessive (PHPVAR)), OMIM:221900)
| Official abbreviation |
PHPVAR |
| Name |
vitreous, primary, hyperplastic, persistent, autosomal recessive (PHPVAR) |
| OMIM ID |
221900 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
ATOH7 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|