Search Ontology:
Human Disease
PEHO syndrome
- Term ID
- DOID:0080539
- Synonyms
-
- Definition
- A brain disease that is characterized by extreme cerebellar atrophy due to almost total granule neuron loss. (4)
- References
-
- GARD:4264
- MESH:C536317
- MIM:260565
- Ontology
- Human Disease ( DOID:0080539 )
- is a type of
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Genes Involved
| Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
|---|---|---|---|---|
| ZNHIT3 | PEHO syndrome | PEHO syndrome | 260565 |
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Zebrafish Models