ISCA-37448-Loss

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red ISCA-37448-Loss Region in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.780

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • ClinGen
  • ClinGen
Phenotypes
  • Chromosome 15q11.2 deletion syndrome, MIM#615656

Red ISCA-37448-Loss Region in Common deletion and duplication syndromes


Version 0.158

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • ClinGen
Phenotypes
  • Chromosome 15q11.2 deletion syndrome, MIM#615656