citrullinemia Disease Ontology Browser

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Disease Ontology Browser

citrullinemia (DOID:9273)
Alliance: disease page
Synonyms: ASS deficiency; deficiency of citrulline-aspartate ligase
Alt IDs: ICD10CM:E72.23, MESH:D020159, NCI:C84639, ORDO:187, UMLS_CUI:C0175683
Definition: An inherited urea cycle disorder that involves the accumulation of ammonia and other toxic substances in the blood.

Disease References using Mouse Models (4)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Ass1tm1Bay/Ass1tm1Bay	involves: 129S7/SvEvBrd * C57BL/6J	J:18326	View
Ass1fold/Ass1fold	B6Ei.P-Ass1^fold/GrsrJ	J:165341	View
Ass1bar/Ass1bar	B6.BAR-Ass1^bar	J:165341	View
Ass1fold/Ass1fold	involves: C57BL/6JEiJ * P/J	J:165341	View
Ass1bar/Ass1bar	FVB.BAR-Ass1^bar	J:165341	View
Ass1bar/Ass1fold	involves: C57BL/6Ei * C57BL/6J * OF1 * P/J	J:165341	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Gpd2tm1Tka/Gpd2tm1Tka Slc25a13tm1Lct/Slc25a13tm1Lct	B6.Cg-Gpd2^tm1Tka Slc25a13^tm1Lct	J:124766	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Slc25a13tm1Lct/Slc25a13tm1Lct	either: 129/Sv-Slc25a13^tm1Lct or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	J:87578	View