Disease #00042
| Official abbreviation |
PRLMNS |
| Name |
Perlman syndrome |
| OMIM ID |
267000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 1 gene |
DIS3L2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|
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