Disease #00382 (MCAP (megalencephaly-capillary malformation-polymicrogyria syndrome, somatic (MCAP)), OMIM:602501)
| Official abbreviation |
MCAP |
| Name |
megalencephaly-capillary malformation-polymicrogyria syndrome, somatic (MCAP) |
| OMIM ID |
602501 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PIK3CA |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-05-14 14:25:00 +02:00 (CEST) |
| Date last edited |
N/A |
|
