Condition: Abnormality of the middle phalanx of the 5th finger
rs864309486
in
GMNN
gene and
Abnormality of the middle phalanx of the 5th finger
PMID 26637980
2015 De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.