Disease #04371 (ZLS2 (Zimmermann-Laband syndrome, type 2 (ZLS2)), OMIM:616455)

Official abbreviation ZLS2
Name Zimmermann-Laband syndrome, type 2 (ZLS2)
OMIM ID 616455
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ATP6V1B2
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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00111405 S_065 PubMed: Popp 2017, Journal: Popp 2017 - F no - - - - - - ZLS2 Severe ID, hypotonia, microcephaly, three seizures ATP6V1B2 ATP6V1B2 1 1 Bernt Popp
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