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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