Disease #00449 (MLDB (leukodystrophy, metachromatic, due to saposin-B deficiency), OMIM:249900)
Official abbreviation |
MLDB |
Name |
leukodystrophy, metachromatic, due to saposin-B deficiency |
OMIM ID |
249900 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
32 |
Phenotype entries for this disease |
31 |
Associated with 1 gene |
PSAP |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-07-09 21:18:32 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|