MCM7

minichromosome maintenance complex component 7
OMIM: 600592, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber MCM7 in Severe microcephaly

Level 3: DNA repair disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 5.7
Latest signed off version: v5.0 (1 May 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Meier-Gorlin syndrome
  • Microcephaly
  • Intellectual disability