Disease #03280 (WMS4 (Weill-Marchesani 4 syndrome, recessive), OMIM:613195)

Official abbreviation WMS4
Name Weill-Marchesani 4 syndrome, recessive
OMIM ID 613195
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ADAMTS17
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

3 entries on 1 page. Showing entries 1 - 3.
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00088064 - - - F yes Turkey kurd - - - - WMS4 Proportionate short stature, brachydactyly, joint stiffness and microspherophakia ADAMTS10 ADAMTS10 1 1 Oliver Brandau
00088065 - - - F no Germany - - - - - WMS4 - ADAMTS10 ADAMTS10 2 1 Andreas Laner
00088067 - - - M ? Germany - - - - - WMS4 Complex eyemalformation, congential cataract, congenital keratektasie, megalocornea, congenital heart defect, microsomia ADAMTS10 ADAMTS10 1 1 Andreas Laner
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