Lissencephaly type 1 due to doublecortin gene mutation

Lissencephaly type 1 due to doublecortin gene mutation (disorder)

active

Code	`715780008`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20160731

Synonyms

X-linked lissencephaly type 1

Parents (4)

363070008Developmental hereditary disorder disorder
363235000Hereditary disorder of nervous system disorder
253147000Type 1 lissencephaly disorder
128430005X-linked hereditary disease disorder

Children (0)

None (leaf concept).