Disease #01978 (LIS2 (lissencephaly, type 2 (LIS-2)), OMIM:257320)

Official abbreviation LIS2
Name lissencephaly, type 2 (LIS-2)
OMIM ID 257320
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene RELN
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00080846 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - LIS2 Lissencephaly 2 (Norman-Roberts type) (OMIM:257320) RELN RELN 1 1 Daniel Trujillano
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