FGF3

fibroblast growth factor 3
OMIM: 164950, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green FGF3 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, congenital with inner ear agenesis, microtia, and microdontia, MIM#610706

Green FGF3 in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.194

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance Deafness Flagship
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, congenital with inner ear agenesis, microtia, and microdontia, MIM# 610706

Red FGF3 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • Deafness, congenital with inner ear agenesis, microtia, and microdontia, MIM#610706

Green FGF3 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • BabySeq Category A gene
  • Expert Review Green
Phenotypes
  • Deafness, congenital with inner ear agenesis, microtia, and microdontia

Green FGF3 in Fetal anomalies


Version 1.255

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
  • Genetic Health Queensland
Phenotypes
  • Deafness, congenital with inner ear agenesis, microtia, and microdontia, MIM#610706

Green FGF3 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.113

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • BabySeq Category A gene
Phenotypes
  • Deafness, congenital with inner ear agenesis, microtia, and microdontia, MIM# 610706
Tags
  • deafness