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
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