Disease #00091 (HP (Hereditary Pancreatitis), OMIM:167800)
Official abbreviation |
HP |
Name |
Hereditary Pancreatitis |
OMIM ID |
167800 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
PRSS1 |
Associated tissues |
pancreas |
Disease features |
- |
Remarks |
- |
Individuals
|
|