Disease #00656
| Official abbreviation |
165200 |
| Name |
OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS, 165200 |
| OMIM ID |
165200 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
OMIM description: Lees et al. (1964) described a kindred in 5 generations of which 12 males and 3 females were affected with optic neuritis accompanied in some by neurologic manifestations resembling disseminated sclerosis. One had ataxia, right leg weakness and dysarthria. Another developed left hemiparesis during a 2-week period and then recovered partially. Went (1974) expressed the opinion that this kindred is an example of Leber optic atrophy (535000) and not a separate entity |
|
|
