Disease #05425 (PEBAT (encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum (PEBAT)), OMIM:617193)
| Official abbreviation |
PEBAT |
| Name |
encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum (PEBAT) |
| OMIM ID |
617193 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
9 |
| Phenotype entries for this disease |
9 |
| Associated with 1 gene |
TBCD |
| Associated tissues |
- |
| Disease features |
autosomal recessive |
| Remarks |
- |
| Date created |
2018-05-04 16:06:21 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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