SPARCL1

SPARC like 1
OMIM: 606041, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SPARCL1 in Corneal Dystrophy


Level 2: Ophthalmological disorders
Version 1.11

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Corneal dystrophy, MONDO:0018102

Red SPARCL1 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Corneal dystrophy, MONDO:0018102