Disease #04343 (CBAS-5 (bile acid synthesis defect?, congenital, type 5 (CBAS-5)), OMIM:616278)
| Official abbreviation |
CBAS-5 |
| Name |
bile acid synthesis defect?, congenital, type 5 (CBAS-5) |
| OMIM ID |
616278 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ABCD3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
N/A |
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