Disease #03307 (ARHR2 (rickets, hypophosphatemic, autosomal recessive, type 2 (ARHR-2)), OMIM:613312)
| Official abbreviation |
ARHR2 |
| Name |
rickets, hypophosphatemic, autosomal recessive, type 2 (ARHR-2) |
| OMIM ID |
613312 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
ENPP1 |
| 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
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