Disease #00891 (NSHPT (hyperparathyroidism, severe, neonatal (NSHPT)), OMIM:239200)
| Official abbreviation |
NSHPT |
| Name |
hyperparathyroidism, severe, neonatal (NSHPT) |
| OMIM ID |
239200 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
45 |
| Phenotype entries for this disease |
28 |
| Associated with 1 gene |
CASR |
| Associated tissues |
- |
| Disease features |
autosomal dominant/autosomal recessive |
| 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
|