Disease #04621 (HLD-11 (leukodystrophy, hypomyelinating, type 11 (HLD-11)), OMIM:616494)
Official abbreviation |
HLD-11 |
Name |
leukodystrophy, hypomyelinating, type 11 (HLD-11) |
OMIM ID |
616494 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
POLR1C |
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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