Disease #05260 (CAVIPMR (atrophy, cerebellar, visual impairment, psychomotor retardation (CAVIPMR)), OMIM:616875)
| Official abbreviation |
CAVIPMR |
| Name |
atrophy, cerebellar, visual impairment, psychomotor retardation (CAVIPMR) |
| OMIM ID |
616875 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
EMC1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-04-11 14:50:42 +02:00 (CEST) |
| Date last edited |
2020-11-13 14:32:57 +01:00 (CET) |
Individuals
|