Disease #00878 (Crigler-Najjar I (Crigler-Najjar syndrome, type I), OMIM:218800)
| Official abbreviation |
Crigler-Najjar I |
| Name |
Crigler-Najjar syndrome, type I |
| OMIM ID |
218800 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
8 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
UGT1A1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2022-05-30 21:30:33 +02:00 (CEST) |
Individuals
|