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Echinobase
Summary Literature (0)
MIM:613610 - CRANIOECTODERMAL DYSPLASIA 2; CED2

Echinobase Genes: wdr35

Human Disease Resource: OMIM


Disease Ontology (DO):
DOID:0050577 - Sensenbrenner syndrome
DOID:0080804 - cranioectodermal dysplasia 2