PanelApp (stage)
  1. Genes and Genomic Entities
  2. FEZF1

FEZF1

FEZ family zinc finger 1
OMIM: 613301, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber FEZF1 in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.293

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Hypogonadotropic hypogonadism 22, with or without anosmia 616030

Amber FEZF1 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Hypogonadotropic hypogonadism 22, with or without anosmia, MIM# 616030

Amber FEZF1 in Primary Ovarian Insufficiency_Premature Ovarian Failure

Level 3: Gonadal and sex development disorders
Level 2: Endocrine disorders
Version 0.328

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Royal Melbourne Hospital
Phenotypes
  • Hypogonadotropic hypogonadism 22, with or without anosmia 616030

Red FEZF1 in Fetal anomalies


Version 1.255

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Genomics England PanelApp
Phenotypes
  • Hypogonadotropic hypogonadism 22, with or without anosmia, MIM# 616030