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 |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
ABCD3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|