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
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