has material basis in germline mutation in EIF2AK3 syndromic disease diabetes mellitus autosomal recessive disease Wolcott-Rallison syndrome https://github.com/monarch-initiative/mondo/issues/4948 https://github.com/monarch-initiative/mondo/issues/5723 https://rarediseases.info.nih.gov/diseases/5589/epiphyseal-dysplasia-multiple-with-early-onset-diabetes-mellitus https://www.malacards.org/card/epiphyseal_dysplasia_multiple_with_early_onset_diabetes_mellitus_2 OMIM:226980 icd11.foundation:2096915129 Wolcott Rallison syndrome Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure. NCIT:C131007 MONDO:0009192 Iddm-Med syndrome UMLS:C0432217 GARD:0005589 early-onset diabetes mellitus with multiple epiphyseal dysplasia MESH:C536739 Wolcott-Rallison syndrome Med-Iddm syndrome MED-IDDM syndrome epiphyseal dysplasia, multiple, with early-onset diabetes mellitus DOID:0090060 Orphanet:1667 epiphyseal dysplasia multiple with early-onset diabetes mellitus MEDGEN:140926 IDDM-MED syndrome SCTID:254066006 WRS spondyloepiphyseal dysplasia