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Date	Panel	Item	Activity
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07 Jun 2022	Inherited bleeding disorders v1.172	F13B	Arina Puzriakova Added comment: Comment on mode of inheritance: Updated from 'Monoallelic' to 'Both mono- and biallelic'. Although patients primarily present with biallelic variants, there is also evidence of monoallelic disease albeit in fewer frequency, likely due to the mild extent of symptoms resulting in many carriers going undetected until exposed to trauma.
07 Jun 2022	Inherited bleeding disorders v1.172	F13B	Arina Puzriakova Mode of inheritance for gene: F13B was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
07 Jun 2022	Inherited bleeding disorders v1.171	F13B	Arina Puzriakova Phenotypes for gene: F13B were changed from Factor XIII deficiency; VENOUS THROMBOSIS, SUSCEPTIBILITY TO to Factor XIIIB deficiency, OMIM:613235
19 Dec 2016	Inherited bleeding disorders	F13B	Louise Daugherty reviewed F13B
19 Dec 2016	Inherited bleeding disorders	F13B	BRIDGE consortium reviewed F13B