Disease #00089
Official abbreviation |
605814 |
Name |
Citrullinemia, type II, neonatal-onset, 605814 (3) |
OMIM ID |
605814 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
SLC25A13 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|