Disease #00947 (SHFM3 (split-hand/foot malformation, type 3, gene duplication syndrome (SHFM3)), OMIM:246560)

Official abbreviation SHFM3
Name split-hand/foot malformation, type 3, gene duplication syndrome (SHFM3)
OMIM ID 246560
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 10
Phenotype entries for this disease 10
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks linked to FGF8 Cova ESHG2020 PL2.5
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-10-18 22:36:33 +02:00 (CEST)


Individuals

10 entries on 1 page. Showing entries 1 - 10.
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00183243 - - - - - - - - - - - SHFM3 - BTRC BTRC 1 1 Fabienne Escande
00184296 - - - M - - - - - - - SHFM3 - BTRC BTRC 1 1 Fabienne Escande
00184297 - - - - - - - - - - - SHFM3 - BTRC BTRC 1 1 Fabienne Escande
00184298 - - - - - - - - - - - SHFM3 - BTRC BTRC 1 1 Fabienne Escande
00184299 - - - - - - - - - - - SHFM3 - BTRC BTRC 1 1 Fabienne Escande
00184300 - - - - - - - - - - - SHFM3 - BTRC BTRC 1 1 Fabienne Escande
00184301 - - - - - - - - - - - SHFM3 - BTRC BTRC 1 1 Fabienne Escande
00234326 23-II-1 - - M no Japan - - - - - SHFM3 , split hand, split foot - - 1 1 Kaori Yamoto
00234327 24-II-1 - - F no Japan - - - - - SHFM3 Clinodactyly - - 1 2 Kaori Yamoto
00234328 25-II-2 - - F no Japan - - - - - SHFM3 - - - 1 1 Kaori Yamoto
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