lissencephaly with cerebellar hypoplasia type E

Go to external page http://purl.obolibrary.org/obo/MONDO_0015038


Lissencephaly with cerebellar hypoplasia type E (LCHe) is a form of lissencephaly with cerebellar hypoplasia, characterized by an abrupt transition from agyria to gyral simplification, near the boundary between frontal and parietal cortex, microcephaly (B1 3 SD) and brainstem hypoplasia. [ Orphanet:100015 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10:Q04.3 (Orphanet:100015)
  • Orphanet:100015 (MONDO:equivalentTo)
  • UMLS:CN228904 (MONDO:equivalentTo)
Subsets

ordo_malformation_syndrome

definition

Lissencephaly with cerebellar hypoplasia type E (LCHe) is a form of lissencephaly with cerebellar hypoplasia, characterized by an abrupt transition from agyria to gyral simplification, near the boundary between frontal and parietal cortex, microcephaly (B1 3 SD) and brainstem hypoplasia.

exactMatch

http://www.orpha.net/ORDO/Orphanet_100015

http://linkedlifedata.com/resource/umls/id/CN228904

id

MONDO:0015038

Term relations