SLC27A4

solute carrier family 27 member 4
OMIM: 604194
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ICHTHYOSIS PREMATURITY SYNDROME 608649
R-numbers: R21, R412
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ICHTHYOSIS PREMATURITY SYNDROME
R-numbers: R165
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ichthyosis prematurity syndrome, OMIM:608649
R-numbers: R166
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ichthyosis prematurity syndrome