HOXA4

homeobox A4
OMIM: 142953, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red HOXA4 in Congenital anomalies of the kidney and urinary tract (CAKUT)


Level 2: Renal and urinary tract disorders
Version 0.204

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • 2 reviews Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Red

    Red HOXA4 in Mendeliome


    Version 1.4601

    2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Microtia with meatal atresia and conductive deafness MONDO:0009634, HOXA4-related