Disease #04139 (MPPH-2 (megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome, type 2 (MPPH-2)), OMIM:615937)
| Official abbreviation |
MPPH-2 |
| Name |
megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome, type 2 (MPPH-2) |
| OMIM ID |
615937 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
AKT3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
