Disease #05853 (CHANDS (CHAND syndrome), OMIM:214350)
| Official abbreviation |
CHANDS |
| Name |
CHAND syndrome |
| OMIM ID |
214350 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
RIPK4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-10-15 08:50:59 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|