Disease #04536 (LIS6 (lissencephaly, type 6, with microcephaly (LIS-6)), OMIM:616212)

Official abbreviation LIS6
Name lissencephaly, type 6, with microcephaly (LIS-6)
OMIM ID 616212
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 KATNB1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00376166 Case 1 Peluso et al., Genes (Basel) 2021 - F yes India - - - - - LIS6 HP:0000252, HP:0011327, HP:0012766, HP:0002536, HP:0025100, HP:0032391, HP:0006891, HP:0000666, HP:0007703, HP:0001488, HP:0011681, HP:0001684, HP:0004209, HP:0005709, HP:0001510, HP:0001263, HP:0012712 - KATNB1 1 1 Stefano Giuseppe Caraffi
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