Disease #04670 (HMNR8 (cataract, congenital?neuronopathy, distal hereditary motor, autosomal recessive,type 8), OMIM:618912)
| Official abbreviation |
HMNR8 |
| Name |
cataract, congenital?neuronopathy, distal hereditary motor, autosomal recessive,type 8 |
| OMIM ID |
618912 |
| 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 |
SORD |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
2026-03-06 19:35:50 +01:00 (CET) |
Individuals
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