HGF

hepatocyte growth factor
OMIM: 142409, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green HGF in Mendeliome


Version 1.4541

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal recessive 39, MIM# 608265
  • Lymphoedema, MONDO:0019297, HGF-related
Tags
  • deep intronic
  • founder

Green HGF in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.332

1 review Unknown
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance Deafness Flagship
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal recessive 39, MIM# 608265

Green HGF in Lymphoedema

Level 3: Lymphatic Disorders
Level 2: Cardiovascular disorders
Version 0.32

Component of the following Super Panels:

  • Vascular Malformations SuperPanel
  • 1 review Unknown
    Sources
    • Expert Review Green
    • Literature
    • Expert list

    Green HGF in Additional findings_Paediatric


    Level 2: Screening
    Version 0.280

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category C gene
    Phenotypes
    • Deafness, autosomal recessive

    Green HGF in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.147

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category C gene
    Phenotypes
    • Deafness, autosomal recessive 39, MIM# 608265
    Tags
    • deep intronic
    • founder
    • deafness