Disease #00275 (MOPD-2 (microcephalic osteodysplastic primordial dwarfism, type II (MOPD-2)), OMIM:210720)
| Official abbreviation |
MOPD-2 |
| Name |
microcephalic osteodysplastic primordial dwarfism, type II (MOPD-2) |
| OMIM ID |
210720 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PCNT |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-11-22 15:29:13 +01:00 (CET) |
| Date last edited |
N/A |
|
