A rare autosomal dominant inherited disorder caused by mutations in the FGFR3 gene. It is characterized by premature fusion of cranial bones, resulting in head shape abnormalities, flattened cheekbones, and wide-set eyes. [ ]

Synonyms: Muenke Syndrome

This is just here as a test because I lose it

Term information

Preferred Name

Muenke Syndrome

Semantic Type

Disease or Syndrome

UMLS CUI

C1864436

code

C84904