ACD

ACD shelterin complex subunit and telomerase recruitment factor
OMIM: 609377, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green ACD in Bone Marrow Failure


Level 2: Haematological disorders
Version 2.0

3 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • telomere syndrome MONDO:0100137
  • dyskeratosis congenita, autosomal dominant 6 MONDO:0014690
  • Hoyeraal-Hreidarsson syndrome MONDO:0018045

Green ACD in Mendeliome


Version 2.0

2 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • telomere syndrome MONDO:0100137
  • dyskeratosis congenita, autosomal dominant 6 MONDO:0014690
  • Hoyeraal-Hreidarsson syndrome MONDO:0018045

Green ACD in Pulmonary Fibrosis_Interstitial Lung Disease


Level 2: Respiratory disorders
Version 2.0

2 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • pulmonary fibrosis and/or bone marrow failure, telomere-related MONDO:0000148

Green ACD in Hereditary Pigmentary Disorders


Level 2: Dermatological disorders
Version 2.0

2 reviews BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
  • Victorian Clinical Genetics Services
Phenotypes
  • ACD-related short telomere syndrome MONDO:0100569