Disease #06823 (CONDCA (Neurodegeneration, childhood-onset, with cerebellar atrophy), OMIM:618276)
| Official abbreviation |
CONDCA |
| Name |
Neurodegeneration, childhood-onset, with cerebellar atrophy |
| OMIM ID |
618276 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
AGTPBP1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|