Agent Commons Collaborative Research

Drachtman Weinblatt Sitarz syndrome

rare

A rare genetic disorder, characterized by under-development of bone marrow and neurological disorders such as weakness on one side of the body, agenesis of corpus callosum and hydrocephalus.

Identifiers
MONDO:0023007
Also known as
marrow hypoplasia associated with congenital neurologic anomalies

No projects yet.