Disease #01768 (SHFM6 (split-hand/foot malformation, type 6 (SHFM-6)), OMIM:225300)

Official abbreviation SHFM6
Name split-hand/foot malformation, type 6 (SHFM-6)
OMIM ID 225300
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene WNT10B
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

6 entries on 1 page. Showing entries 1 - 6.
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00079873 - - - - yes Pakistan Pashtun - 1 - - SHFM6 Affected individuals in this large consanguineous family showed variable prototypes of split hand foot malformation HOXD8 HOXD8, HOXD9 2 15 Irfan Ullah
00231002 32-II-1 - - F no Japan - - - - - SHFM6 split hand, split foot, syndactyly WNT10B WNT10B 2 2 Kaori Yamoto
00231003 33-II-1 - - F no Japan - - - - - SHFM6 split hand, syndactyly WNT10B WNT10B 1 1 Kaori Yamoto
00231004 34-II-1 - - M no Japan - - - - - SHFM6 split foot, ventricular septal defect WNT10B WNT10B 1 1 Kaori Yamoto
00231005 35-II-1 - - M no Japan - - - - - SHFM6 split foot, polydactyly, Microphthalmia, cryptorchidism, global developmental delay WNT10B PORCN, WNT10B 2 1 Kaori Yamoto
00235305 32-II-2 - - M no Japan - - - - - SHFM6 split hand, syndactyly - WNT10B 2 1 Kaori Yamoto
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