Disease #00342 (LISX1;SCLH (lissencephaly, X-linked, type 1 (subcortical laminar heterotopia (SCLH))), OMIM:300067)

Official abbreviation LISX1;SCLH
Name lissencephaly, X-linked, type 1 (subcortical laminar heterotopia (SCLH))
OMIM ID 300067
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene DCX
Associated tissues -
Disease features -
Remarks -
Date created 2014-03-12 20:58:51 +01:00 (CET)
Date last edited 2024-11-22 20:39:22 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00016317 - PubMed: Della Mina et al 2014 - F - - - - - - - LISX1;SCLH diagnosis subcortical laminar heterotopia, X-linked, included DCX, SHANK3 DCX, SHANK3 2 1 Lab Zuffardi
00380936 178906 - - F no Germany - - - - - LISX1;SCLH Double-Cortex syndrome with Seizure, Motor seizure, Myoclonic seizure DCX DCX 1 1 Andreas Laner
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