LIPC

lipase C, hepatic type
OMIM: 151670, ClinGen, DECIPHER

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green LIPC in Mendeliome


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
  • Victorian Clinical Genetics Services
Phenotypes
  • Hepatic lipase deficiency MIM#614025
  • Hyperlipidemia due to hepatic triglyceride lipase deficiency, MONDO:0013533

Green LIPC in Dyslipidaemia


Level 2: Endocrine disorders; Cardiovascular disorders
Version 1.0

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Hepatic lipase deficiency MIM#614025
  • Inherited mixed hyperlipidaemias
  • hyperalphalipoproteinemia

Red LIPC in Monogenic Diabetes


Level 2: Endocrine disorders
Version 1.0

1 review Unknown
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • {Diabetes mellitus, noninsulin-dependent}, MIM#125853

Green LIPC in Mackenzie's Mission_Reproductive Carrier Screening


Level 2: Screening
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Hepatic lipase deficiency, 614025 (3)

Red LIPC in Prepair 1000+


Level 2: Screening
Version 3.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Mackenzie's Mission
Phenotypes
  • Hepatic lipase deficiency, MIM# 614025

Green LIPC in Transplant Co-Morbidity


Level 2: Screening
Version 1.0

0 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Inherited mixed hyperlipidaemias
  • Hepatic lipase deficiency MIM#614025
  • hyperalphalipoproteinemia