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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