Disease #06629 (GINGF5 (fibromatosis, gingival, type 5), OMIM:617626)

Official abbreviation GINGF5
Name fibromatosis, gingival, type 5
OMIM ID 617626
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene REST
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2023-01-05 14:47:46 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00416320 FamPat1 PubMed: Rahikkala 2022, Journal: Rahikkala 2022 2-generation family, 3 affected (father/2 daughters) F no Finland - - - - - GINGF5 - - REST 1 3 Elisa Rahikkala
00420046 FamPat2 PubMed: Rahikkala 2022, Journal: Rahikkala 2022 sister F no Finland - - - - - GINGF5 - - REST 1 1 Elisa Rahikkala
00420048 FamPat3 PubMed: Rahikkala 2022, Journal: Rahikkala 2022 father M no Finland - - - - - GINGF5 - - REST 1 1 Elisa Rahikkala
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