lissencephaly with cerebellar hypoplasia type F

Go to external page http://purl.obolibrary.org/obo/MONDO_0015039


Lissencephaly with cerebellar hypoplasia type F (LCHf) is a severe form of lissencephaly with cerebellar hypoplasia, characterized by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum. [ Orphanet:100016 ]

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:100016 (MONDO:equivalentTo)
  • UMLS:CN228905 (MONDO:equivalentTo)
  • ICD10:Q04.3 (Orphanet:100016)
  • SCTID:715822007 (MONDO:equivalentTo)
  • UMLS:C4274989 (MONDO:equivalentTo)
Subsets

ordo_malformation_syndrome

definition

Lissencephaly with cerebellar hypoplasia type F (LCHf) is a severe form of lissencephaly with cerebellar hypoplasia, characterized by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum.

exactMatch

http://identifiers.org/snomedct/715822007

http://www.orpha.net/ORDO/Orphanet_100016

http://linkedlifedata.com/resource/umls/id/CN228905

http://linkedlifedata.com/resource/umls/id/C4274989

id

MONDO:0015039

Term relations