MAX

MYC associated factor X
OMIM: 154950
PanelMode of inheritanceDetails
4 panels
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Familial Pheochromocytoma, adrenal
R-numbers: R359
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
{Pheochromocytoma, susceptibility to}, OMIM:171300
R-numbers: R223
Signed-off version 3.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
{Pheochromocytoma, susceptibility to}, OMIM:171300, Hereditary Paraganglioma-Pheochromocytoma Syndrome
Component of the following Super Panels:
  • - Cerebral malformation
Signed-off version 3.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Polydactyly-macrocephaly syndrome, OMIM:620712