Disease #01496 (ADLD (leukodystrophy, adult-onset, autosomal dominant), OMIM:169500)
| Official abbreviation |
ADLD |
| Name |
leukodystrophy, adult-onset, autosomal dominant |
| OMIM ID |
169500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
6 |
| Phenotype entries for this disease |
6 |
| Associated with 1 gene |
LMNB1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-09-19 21:03:07 +02:00 (CEST) |
Individuals
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