Disease #00483
Official abbreviation |
PRLTS2 |
Name |
PERRAULT SYNDROME 2; PRLTS2 |
OMIM ID |
614926 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
HARS2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|