Disease #03288 (F13AD (deficiency, factor XIII (A subunit) (F13AD)), OMIM:613225)

Official abbreviation F13AD
Name deficiency, factor XIII (A subunit) (F13AD)
OMIM ID 613225
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene F13A1
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

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00305946 45 - - M - China - - - - - F13AD - F13A1 F13A1 2 1 Sha Hong
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