PRDM12

PR/SET domain 12
OMIM: 616458
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neuropathy, hereditary sensory and autonomic, type VIII OMIM:616488, congenital insensitivity to pain-hypohidrosis syndrome MONDO:0014662
R-numbers: R78
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neuropathy, hereditary sensory and autonomic, type VIII OMIM:616488, congenital insensitivity to pain-hypohidrosis syndrome MONDO:0014662