Disease #00097 (CTLN2 (Citrullinemia, Type II, Adult-Onset), OMIM:603471)
Official abbreviation |
CTLN2 |
Name |
Citrullinemia, Type II, Adult-Onset |
OMIM ID |
603471 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SLC25A13 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-03-31 15:58:53 +08:00 (CST) |
Date last edited |
N/A |
Individuals
|
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