Disease #01035 (SYNS2 (synostoses syndrome, multiple, type 2 (SYNS-2)), OMIM:610017)

Official abbreviation SYNS2
Name synostoses syndrome, multiple, type 2 (SYNS-2)
OMIM ID 610017
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene GDF5
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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00375525 - - - - - - - - - - - SYNS2 - GDF5 GDF5 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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