Disease #04636 (HLD-10 (leukodystrophy, hypomyelinating, type 10 (HLD-10)), OMIM:616420)
| Official abbreviation |
HLD-10 |
| Name |
leukodystrophy, hypomyelinating, type 10 (HLD-10) |
| OMIM ID |
616420 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PYCR2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
N/A |
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