Disease #00805 (MLC2A (leukoencephalopathy, megalencephalic, with subcortical cysts, type 2A (MLC2A)), OMIM:613925)
Official abbreviation |
MLC2A |
Name |
leukoencephalopathy, megalencephalic, with subcortical cysts, type 2A (MLC2A) |
OMIM ID |
613925 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
HEPACAM |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-05-18 10:06:49 +02:00 (CEST) |
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