SPARCL1:Ensemblv90

SPARC like 1
OMIM: 606041, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red SPARCL1 in Corneal Dystrophy


Level 2: Ophthalmological disorders
Version 1.13

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

Red SPARCL1 in Mendeliome


Version 1.3802

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

Red SPARCL1 in Corneal Dystrophy


Level 2: Ophthalmological disorders
Version 2.0

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