ACAN

aggrecan
OMIM: 155760, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green ACAN in Skeletal Dysplasia_Fetal


Level 2: Skeletal disorders
Version 0.223

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Spondyloepimetaphyseal dysplasia, aggrecan type, OMIM# 612813
  • Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans, OMIM# 165800

Green ACAN in Mendeliome


Version 1.1902

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans, OMIM# 165800
  • Spondyloepimetaphyseal dysplasia, aggrecan type 612813

Green ACAN in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.285

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
  • Expert Review Green
  • Radboud University Medical Center, Nijmegen
  • NHS GMS
  • Emory Genetics Laboratory
Phenotypes
  • Spondyloepiphyseal dysplasia, Kimberley type 608361
  • Osteochondritis dissecans, short stature, and early-onset osteoarthritis 165800
  • Spondyloepimetaphyseal dysplasia, aggrecan type 61283

Green ACAN in Growth failure


Version 1.76

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans, MIM# 165800
  • Spondyloepimetaphyseal dysplasia, aggrecan type, MIM# 612813

Green ACAN in Fetal anomalies


Version 1.255

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Spondyloepimetaphyseal dysplasia, aggrecan type, OMIM# 612813
  • Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans, OMIM# 165800