Disease #00250 (hypophosphatemic rickets, X-linked recessive (HPXR), OMIM:300554)
Official abbreviation |
- |
Name |
hypophosphatemic rickets, X-linked recessive (HPXR) |
OMIM ID |
300554 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
CLCN5 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-10-20 13:24:02 +02:00 (CEST) |
Date last edited |
N/A |
|
|