Disease #05070 (PRIMS (Primrose syndrome (PRIMS)), OMIM:259050)
| Official abbreviation |
PRIMS |
| Name |
Primrose syndrome (PRIMS) |
| OMIM ID |
259050 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
12 |
| Phenotype entries for this disease |
12 |
| Associated with 1 gene |
ZBTB20 |
| Associated tissues |
- |
| Disease features |
autosomal dominant; recognizable facial features, macrocephaly, mental retardation, enlarged and calcified external ears, sparse body hair, distal muscle wasting |
| Remarks |
- |
| Date created |
2015-09-23 11:00:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|