Disease #02031 (PHA-1B (pseudohypoaldosteronism type 1 autosomal recessive (PHA-1B)), OMIM:264350)
| Official abbreviation |
PHA-1B |
| Name |
pseudohypoaldosteronism type 1 autosomal recessive (PHA-1B) |
| OMIM ID |
264350 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 3 genes |
SCNN1A, SCNN1B, SCNN1G |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
