Disease #06833 (WSKA (Weiss-Kruszka syndrome), OMIM:618619)

Official abbreviation WSKA
Name Weiss-Kruszka syndrome
OMIM ID 618619
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 ZNF462
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00447968 - - - ? yes China - - - - - WSKA Agenesis of corpus callosum with Interhemispheric cyst ZNF462 ZNF462 1 3 Chunxiao Han
00447969 - - - M - China - - - - - WSKA developmental delay, Autistic behavior, EEG abnormality ZNF462 ZNF462 1 1 Chunxiao Han
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