Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/OMIM/300067
http://purl.bioontology.org/ontology/OMIM/300067
Preferred Name

LISSENCEPHALY, X-LINKED, 1
Synonyms
XLIS
DOUBLE CORTEX SYNDROME
DC SYNDROME
SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED
LISSENCEPHALY AND AGENESIS OF CORPUS CALLOSUM
SUBCORTICAL BAND HETEROTOPIA, X-LINKED
SBH
LISX1
SCLH
Type http://www.w3.org/2002/07/owl#Class

All Properties

altLabel
XLIS
DOUBLE CORTEX SYNDROME
DC SYNDROME
SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED
LISSENCEPHALY AND AGENESIS OF CORPUS CALLOSUM
SUBCORTICAL BAND HETEROTOPIA, X-LINKED
SBH
LISX1
SCLH
See more
See less
prefLabel
LISSENCEPHALY, X-LINKED, 1
Gene Symbol
DCX
DBCN
LISX
Scope Statement
Caused by mutation in the doublecortin gene (DCX, 300121.0001) [MOLECULAR BASIS]
Onset in infancy [MISCELLANEOUS]
Somatic or germline mosaicism may occur [MISCELLANEOUS]
Incomplete penetrance [MISCELLANEOUS]
Highly variable phenotype in females [MISCELLANEOUS]
type
Has manifestation
tui
T047
Gene Locus
Xq22.3-q23
MIMTYPEMEANING
Phenotype description, molecular basis known.
notation
300067
Semantic type UMLS property
Has inheritance type
cui
C1848200
C4551968
C1848070
C1848201
Moved from
600102
OMIM Entry Type
3
OMIM MimType Value
pound
Add comment
Add proposal
Delete Subject Author Type Created
No notes to display