Disease #00573 (PRLMNS (Perlman syndrome (PRLMNS)), OMIM:267000)
Official abbreviation |
PRLMNS |
Name |
Perlman syndrome (PRLMNS) |
OMIM ID |
267000 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
5 |
Phenotype entries for this disease |
5 |
Associated with 1 gene |
DIS3L2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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