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 -


Individuals

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00000552 Yuan-Zong Song et al.(2013) M Malaysia - - - - CTLN2 - SLC25A13 SLC25A13 1 1 Nur Aisyah Athirah
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