PanelApp (test)
  1. Genes and Genomic Entities
  2. FGF9:Ensemblv90

FGF9:Ensemblv90

fibroblast growth factor 9
OMIM: 600921, ClinGen, DECIPHER

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Green FGF9 in Craniosynostosis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.73

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Multiple synostoses syndrome 3 MIM#612961

Green FGF9 in Mendeliome


Version 1.3802

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Multiple synostoses syndrome 3, OMIM # 612961
  • Craniosynostosis

Green FGF9 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.365

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review Green
  • NHS GMS
  • Victorian Clinical Genetics Services
Phenotypes
  • Multiple synostoses syndrome type 3 612961

Green FGF9 in Hand and foot malformations


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.80

Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel

    		•  2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert list
    • Expert Review Green
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Multiple synostoses syndrome type 3 612961

    Green FGF9 in Fetal anomalies


    Version 1.482

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Multiple synostoses syndrome 3, OMIM # 612961
    • Craniosynostosis

    Green FGF9 in Craniosynostosis


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 2.0

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green
    Phenotypes
    • Multiple synostoses syndrome 3 MIM#612961

    Green FGF9 in Skeletal dysplasia

    Level 3: Skeletal dysplasias
    Level 2: Skeletal disorders
    Version 1.0

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Victorian Clinical Genetics Services
    • NHS GMS
    • Expert Review Green
    • Expert Review Green
    Phenotypes
    • Multiple synostoses syndrome type 3 612961

    Green FGF9 in Hand and foot malformations


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.0

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green
    • Expert Review Green
    • Expert list
    Phenotypes
    • Multiple synostoses syndrome type 3 612961

    Green FGF9 in Fetal anomalies


    Version 2.0

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Genomics England PanelApp
    • Expert Review Green
    Phenotypes
    • Multiple synostoses syndrome 3, OMIM # 612961
    • Craniosynostosis