LUM

lumican
OMIM: 600616, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red LUM in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Amyotrophic lateral sclerosis

Red LUM in BabyScreen+ newborn screening


Level 2: Screening
Version 1.114

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Amyotrophic lateral sclerosis