Disease #00371 (MCAHS-1 (multiple congenital anomalies, hypotonia, seizures syndrome, type 1 (MCAHS-1)), OMIM:614080)
| Official abbreviation |
MCAHS-1 |
| Name |
multiple congenital anomalies, hypotonia, seizures syndrome, type 1 (MCAHS-1) |
| OMIM ID |
614080 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PIGN |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-04-29 22:18:09 +02:00 (CEST) |
| Date last edited |
N/A |
|
