LMAN2L

lectin, mannose binding 2 like
OMIM: 609552, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber LMAN2L in Mendeliome


Version 1.4220

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Intellectual developmental disorder, autosomal dominant 69 MIM#617863
  • Intellectual developmental disorder, autosomal recessive 52 MIM#616887

Amber LMAN2L in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.638

2 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Intellectual developmental disorder, autosomal dominant 69 MIM#617863
  • Intellectual developmental disorder, autosomal recessive 52 MIM#616887