RSPRY1

ring finger and SPRY domain containing 1
OMIM: 616585
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
PROGRESSIVE SPONDYLOEPIMETAPHYSEAL DYSPLASIA
R-numbers: R100
Signed-off version 4.177
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type, OMIM:616723