Multiple hereditary exostoses type 2

Type

Disease
External link(s)
- IEMbase
Gene
- EXT2 / Exostosin 2
  11p11.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Exostosin-2
Parent entry
- Multiple hereditary exostoses
Child entries
- Seizures, scoliosis, and macrocephaly/microcephaly syndrome
- Potocki-Shaffer syndrome