Mowat-Wilson syndrome

名词 n.

英文释义

名词 n.
  1. A rare genetic disorder typically characterized by Hirschsprung's disease, intellectual disability, epilepsy, delayed growth and motor development, congenital heart disease, genitourinary anomalies, and absence of the corpus callosum. uncountable

词源

Described by David R. Mowat and Meredith J. Wilson in 1998.
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