Disease #05234 (CM1 (malformation, Chiari, type I (CM-1)), OMIM:118420)
| Official abbreviation |
CM1 |
| Name |
malformation, Chiari, type I (CM-1) |
| OMIM ID |
118420 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-03-06 20:17:57 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|