Lymphoedema_nonsyndromic
Gene: HGFEnsemblGeneIds (GRCh38): ENSG00000019991
EnsemblGeneIds (GRCh37): ENSG00000019991
OMIM: 142409, Gene2Phenotype
HGF is in 7 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
More than 10 families reported with childhood- to late-onset lymphoedema.
Sources: LiteratureCreated: 5 Jun 2024, 9:32 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Lymphoedema, MONDO:0019297, HGF-related
Publications
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- Lymphoedema, MONDO:0019297, HGF-related
- OMIM
- 142409
- Clinvar variants
- Variants in HGF
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: hgf has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: hgf has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: HGF was added gene: HGF was added to Lymphoedema_nonsyndromic. Sources: Literature Mode of inheritance for gene: HGF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: HGF were set to 38676400; 38791500 Phenotypes for gene: HGF were set to Lymphoedema, MONDO:0019297, HGF-related Review for gene: HGF was set to GREEN