HMGB3

high mobility group box 3
OMIM: 300193, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red HMGB3 in Mendeliome


Version 1.4516

1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome MONDO:0010485