Disease #05909 (IMPDH2V (activity, enzyme, IMPDH2, variation in), OMIM:617995)

Official abbreviation IMPDH2V
Name activity, enzyme, IMPDH2, variation in
OMIM ID 617995
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene IMPDH2
Associated tissues -
Disease features -
Remarks -
Date created 2021-03-18 09:18:21 +01:00 (CET)
Date last edited N/A

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