Disease #05886 (PEBEL (encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy (PEBEL)))
| Official abbreviation |
PEBEL |
| Name |
encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy (PEBEL) |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
APOA1BP, CARKD |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-12-29 10:54:33 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
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