SPRY1

sprouty RTK signaling antagonist 1
OMIM: 602465, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber SPRY1 in Craniosynostosis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.68

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Craniosynostosis, SPRY1-related, MONDO:0015469

Amber SPRY1 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Craniosynostosis, SPRY1-related, MONDO:0015469