Pituitary hormone deficiency

Gene: FOXH1

Red List (low evidence)

FOXH1 (forkhead box H1)
EnsemblGeneIds (GRCh38): ENSG00000160973
EnsemblGeneIds (GRCh37): ENSG00000160973
OMIM: 603621, Gene2Phenotype
FOXH1 is in 9 panels

0 reviews

History Filter Activity

30 Jan 2019, Gel status: 1

Panel promoted to version 1.0

Ivone Leong (Genomics England Curator)

Ivone Leong: BMP4 is confirmed to be associ

10 Dec 2018, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ivone Leong (Genomics England Curator)

gene: FOXH1 was added gene: FOXH1 was added to Pituitary hormone deficiency. Sources: Illumina TruGenome Clinical Sequencing Services Mode of inheritance for gene: FOXH1 was set to Unknown Phenotypes for gene: FOXH1 were set to Holoprosencephaly; No OMIM number