| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion. (Human Disease Ontology, DOID_12215) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012171 |
| Similar Terms | |
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1 gene mutations causing the oligohydramnios phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| RET | ret proto-oncogene |
