Genomics England
GMS Panels
Panels
Genes and Entities

LHX4

LIM homeobox 4
OMIM: 602146
PanelMode of inheritanceDetails
4 panels
Green
in Congenital hypothyroidism
R-numbers: R145
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
GH, TSH, ACTH, variable gonadotrophin deficiencies, cerebellar abnormalities, anterior pituitary hypoplasia, etopic posterior pituitary, Pituitary hormone deficiency, combined, 4, 262700
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
LHX4-RELATED COMBINED PITUITARY HORMONE DEFICIENCY 290135
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 3.122
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
LHX4-RELATED COMBINED PITUITARY HORMONE DEFICIENCY
Green
in Pituitary hormone deficiency
R-numbers: R159
Signed-off version 3.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Pituitary hormone deficiency, combined, 4 (262700)