Disease #04177 (OMCS (Oliver-McFarlane syndrome (OMCS)), OMIM:275400)
| Official abbreviation |
OMCS |
| Name |
Oliver-McFarlane syndrome (OMCS) |
| OMIM ID |
275400 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
PNPLA6 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-01-27 14:10:39 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|