| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An intestinal disease characterized by a protrusion of abdominal cavity contests through the inguinal canal. (Human Disease Ontology, DOID_0060320) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006077 |
| Similar Terms | |
| Downloads & Tools |
1 gene mutations causing the inguinal hernia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| EFEMP1 | EGF containing fibulin-like extracellular matrix protein 1 |
