Disease #03702 (PCH1B (hypoplasia, pontocerebellar, type 1b (PCH-1B)), OMIM:614678)
Official abbreviation |
PCH1B |
Name |
hypoplasia, pontocerebellar, type 1b (PCH-1B) |
OMIM ID |
614678 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
14 |
Phenotype entries for this disease |
14 |
Associated with 1 gene |
EXOSC3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|