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 -