IVD - Gene browser

IVD

isovaleryl-CoA dehydrogenase

HCNC Approved Symbol: IVD (HGNC:6186)
Genomic Coordinates: 15:40,405,795 - 40,435,947 (15q15.1)
Synonyms: ACAD2, IVDH
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

17Patients

In total, 17 patients were diagnosed with a variant in the IVD gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

017
Patient count

Defective dehydrogenation of isovaleryl coa and butyryl coa: 6 (35.3%)
Patient Count: 6 (35.3%)
% of total patients presenting each phenotype is shown in parentheses.
6 (35.3%)
Acidemia: 6 (35.3%)
Patient Count: 6 (35.3%)
% of total patients presenting each phenotype is shown in parentheses.
6 (35.3%)
Acidosis: 5 (29.4%)
Patient Count: 5 (29.4%)
% of total patients presenting each phenotype is shown in parentheses.
5 (29.4%)
Failure to thrive: 3 (17.6%)
Patient Count: 3 (17.6%)
% of total patients presenting each phenotype is shown in parentheses.
3 (17.6%)
Abnormality of fatty-acid metabolism: 3 (17.6%)
Patient Count: 3 (17.6%)
% of total patients presenting each phenotype is shown in parentheses.
3 (17.6%)