Opsismodysplasia (Q86546): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed an Item
‎Changed an Item
Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
Normal rank

Revision as of 11:57, 15 August 2026

Opsismodysplasia is a skeletal dysplasia characterised by congenital dwarfism (rhizomelic micromelia) and facial dysmorphism (macrocephaly, prominent brow, large fontanels, depressed nasal bridge, a small nose, anteverted nares and a long philtrum, hypertelorism, and exophthalmos).
Language Label Description Also known as
default for all languages
ID_2147268863
    English
    Opsismodysplasia
    Opsismodysplasia is a skeletal dysplasia characterised by congenital dwarfism (rhizomelic micromelia) and facial dysmorphism (macrocephaly, prominent brow, large fontanels, depressed nasal bridge, a small nose, anteverted nares and a long philtrum, hypertelorism, and exophthalmos).

      Statements

      CID11:ID_2147268863
      0 references
      dki-india-ID_2147268863
      0 references
      Concluído
      0 references