Disease #00566 (Wolcott-Rallison syndrome, OMIM:226980)
Official abbreviation |
- |
Name |
Wolcott-Rallison syndrome |
OMIM ID |
226980 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
EIF2AK3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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