Disease #03734 (WMS3 (Weill-Marchesani syndrome, type 3 (WMS-3)), OMIM:614819)

Official abbreviation WMS3
Name Weill-Marchesani syndrome, type 3 (WMS-3)
OMIM ID 614819
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 LTBP2
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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00240057 - - - M - Iran Iranian - - - - WMS3 Ectopia Lentis, microspherophakia, shallow anterior chamber-severe myopia, short stature, brachydactyly, joint stiffness, pulmonary stenosis, aortic stenosis LTBP2 LTBP2 2 1 Ramona Haji-Seyed-Javadi
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