Disease #01714 (YVS (Yunis Varon syndrome (YVS)), OMIM:216340)

Official abbreviation YVS
Name Yunis Varon syndrome (YVS)
OMIM ID 216340
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 FIG4
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

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00385430 187559 - prenatal trio-exom analysis - no Germany - - - - - YVS Fetal cystic hygroma, Increased nuchal translucency, Abnormality of the neck FIG4 FIG4 2 1 Andreas Laner
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