SLC2A10

solute carrier family 2 member 10
OMIM: 606145
PanelMode of inheritanceDetails
4 panels
R-numbers: R336
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Arterial tortuosity syndrome, OMIM:208050
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ARTERIAL TORTUOSITY SYNDROME 208050
R-numbers: R21, R412
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ARTERIAL TORTUOSITY SYNDROME
R-numbers: R125
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Arterial tortuosity syndrome, 208050, Marfan Syndrome, Thoracic Aortic Aneurysm & Dissection (TAAD), and Related Disorders