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Collaborative Research
Diseases
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Disorder of development or morphogenesis
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Hereditary gingival fibromatosis
Fibromatosis, gingival, 5
rare
Identifiers
MONDO:0033493
OMIM:617626
Causal genes
REST
Part of
Hereditary gingival fibromatosis
Also known as
GGF5 · GINGF5
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