Disease #05277 (PEHO (PEHO syndrome (PEHO)), OMIM:260565)
| Official abbreviation |
PEHO |
| Name |
PEHO syndrome (PEHO) |
| OMIM ID |
260565 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
ZNHIT3 |
| Associated tissues |
- |
| Disease features |
progressive encephalopathy (HP:0002448), edema (HP:0000969), hypsarrhythmia (HP:0002521), optic atrophy (HP:0000648) |
| Remarks |
- |
| Date created |
2017-06-02 22:02:29 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|