HGF

hepatocyte growth factor
OMIM: 142409, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green HGF in Lymphoedema_nonsyndromic


Level 2: Cardiovascular disorders
Version 0.39

Component of the following Super Panels:

  • Vascular Malformations SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Lymphoedema, MONDO:0019297, HGF-related

    Green HGF in Mendeliome


    Version 1.1891

    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 1.194

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

    Red HGF in Lymphoedema_syndromic

    Level 3: Lymphatic Disorders
    Level 2: Cardiovascular disorders
    Version 0.12

    Component of the following Super Panels:

  • Vascular Malformations SuperPanel
  • review Unknown
    Sources
    • Expert list

    Green HGF in Deafness_Isolated


    Level 2: Hearing and ear disorders
    Version 1.63

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Melbourne Genomics Health Alliance Deafness Flagship
    • Melbourne Genomics Health Alliance Deafness Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Deafness, autosomal recessive 39, MIM# 608265
    Tags
    • founder

    Green HGF in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

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

    Green HGF in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    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