HOXA13

homeobox A13
OMIM: 142959, ClinGen, DECIPHER

17 panels

Panel Reviews Mode of inheritance Details
17 panels

Green HOXA13 in Congenital anomalies of the kidney and urinary tract (CAKUT)


Level 2: Renal and urinary tract disorders
Version 1.0

1 review Unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green HOXA13 in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hand-foot-uterus syndrome, MIM# 140000

Green HOXA13 in Mendeliome


Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hand-foot-uterus syndrome, MIM# 140000

Green HOXA13 in Polydactyly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green HOXA13 in Radial Ray Abnormalities


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome, MIM# 140000

Green HOXA13 in Skeletal dysplasia

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

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review Green
  • Expert list
  • Radboud University Medical Center, Nijmegen
  • NHS GMS
  • Victorian Clinical Genetics Services
Phenotypes
  • Guttmacher syndrome 176305
  • Hand-foot-uterus syndrome 140000
  • Hand-foot-genital syndrome 140000

Green HOXA13 in Fetal anomalies


Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Genomics England PanelApp
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome, MIM# 140000

Green HOXA13_HFGS_GCN3 STR in Congenital anomalies of the kidney and urinary tract (CAKUT)


Level 2: Renal and urinary tract disorders
Version 1.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
  • Expert Review Green
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome MIM#140000
Tags
  • paediatric-onset

Green HOXA13_HFGS_GCN3 STR in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
  • Expert Review Green
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome MIM#140000
Tags
  • paediatric-onset

Green HOXA13_HFGS_GCN3 STR in Mendeliome


Version 2.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
  • Expert Review Green
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome MIM#140000
Tags
  • paediatric-onset

Green HOXA13_HFGS_GCN3 STR in Polydactyly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
  • Expert Review Green
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome MIM#140000
Tags
  • paediatric-onset

Green HOXA13_HFGS_GCN3 STR in Radial Ray Abnormalities


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
  • Expert Review Green
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome MIM#140000
Tags
  • paediatric-onset

Green HOXA13_HFGS_GCN3 STR in Skeletal dysplasia

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

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
  • Expert Review Green
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome MIM#140000
Tags
  • paediatric-onset

Green HOXA13_HFGS_GCN2 STR in Repeat Disorders


Version 1.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome MIM#140000
Tags
  • paediatric-onset

Green HOXA13_HFGS_GCN3 STR in Repeat Disorders


Version 1.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome MIM#140000
Tags
  • paediatric-onset

Green HOXA13_HFGS_GCN1 STR in Repeat Disorders


Version 1.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome MIM#140000
Tags
  • paediatric-onset

Green HOXA13_HFGS_GCN3 STR in Fetal anomalies


Version 2.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
  • Expert Review Green
  • Expert list
Phenotypes
  • Hand-foot-uterus syndrome MIM#140000
Tags
  • paediatric-onset