Disease: Craniometaphyseal dysplasia, autosomal recessive type ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931244
Disease: Craniometaphyseal dysplasia, autosomal recessive type
Craniometaphyseal dysplasia, autosomal recessive type 		0.200 Biomarker disease MGD Introduction of a Phe377del mutation in ANK creates a mouse model for craniometaphyseal dysplasia. 19257826 2009