Disease #00452 (PSAPD (saposin deficiency, combined (PSAPD)), OMIM:611721)
Official abbreviation |
PSAPD |
Name |
saposin deficiency, combined (PSAPD) |
OMIM ID |
611721 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
PSAP |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-07-09 21:23:07 +02:00 (CEST) |
Date last edited |
2021-06-30 08:22:28 +02:00 (CEST) |
Individuals
|