Disease: MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4693831
Disease: MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE 		0.300 GeneticVariation disease UNIPROT Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders. 28097321 2017
CUI: C4693831
Disease: MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE 		0.300 GeneticVariation disease UNIPROT Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis. 27737959 2016