Disease #02654 (LIS1 (lissencephaly, type 1 (LIS-1)), OMIM:607432)

Official abbreviation LIS1
Name lissencephaly, type 1 (LIS-1)
OMIM ID 607432
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PAFAH1B1
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

2 entries on 1 page. Showing entries 1 - 2.
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00451462 3bINP-041 PubMed: Vela-Amieva 2024 - M no Mexico Mexican - - - - LIS1 Cerebral cortical atrophy, hypsarrhythmia, moderate intellectual disability PAFAH1B1 PAFAH1B1 1 1 Miriam Erandi Reyna-Fabián
00455349 - - - M - China - - - - - LIS1 - PAFAH1B1 PAFAH1B1 1 1 Min Peng
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