Disease #03280

Official abbreviation -
Name syndrome, Weill-Marchesani-like
OMIM ID 613195
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ADAMTS17
Associated tissues -
Disease features -
Remarks -


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00088064 - - - F yes Turkey kurd - 0 - - syndrome, Weill-Marchesani-like Proportionate short stature, brachydactyly, joint stiffness and microspherophakia ADAMTS10 ADAMTS10 1 1 Oliver Brandau
00088065 - - - F no Germany - - 0 - - syndrome, Weill-Marchesani-like - ADAMTS10 ADAMTS10 2 1 Andreas Laner
00088067 - - - M ? Germany - - 0 - - syndrome, Weill-Marchesani-like Complex eyemalformation, congential cataract, congenital keratektasie, megalocornea, congenital heart defect, microsomia ADAMTS10 ADAMTS10 1 1 Andreas Laner
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