Genomics England
GMS Panels
Panels
Genes and Entities
NCAPD2
non-SMC condensin I complex subunit D2
OMIM:
615638
See this entity in PanelApp
Panel
Mode of inheritance
Details
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in
Severe microcephaly
R-numbers:
R88
Signed-off version 6.8
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microcephaly 21, primary, autosomal recessive, OMIM:617983