Disease #01860 (APS1 (polyendocrinopathy autoimmune, type 1, with/without reversible metaphyseal dysplasia (APS1)), OMIM:240300)
| Official abbreviation |
APS1 |
| Name |
polyendocrinopathy autoimmune, type 1, with/without reversible metaphyseal dysplasia (APS1) |
| OMIM ID |
240300 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
18 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
AIRE |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|