About: Factor I Deficiency

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

medical condition

Attributes	Values
rdf:type	Item
owl:sameAs	Factor I Deficiency
description	medical condition (en) медичний стан (uk)
exact match	wds:Q18354630-A9C6C94D-A3D8-421C-BF43-3CAC829E3DD0
exact match	http://www.orpha.net/ORDO/Orphanet_335
Mondo ID	wds:Q18354630-76CA42DE-0CDF-4E93-9B7A-B78F90DDF538
symptoms and signs	wds:Q18354630-C33C38F7-2C17-4AD6-95D5-8A36E7476AB8
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0018060
Mondo ID	MONDO_0018060
symptoms and signs	Hypofibrinogenemia
rdfs:label	Déficit congénital en fibrinogène (fr) Factor I Deficiency (en) 低纖維蛋白原血症 (zh)
skos:prefLabel	Déficit congénital en fibrinogène (fr) Factor I Deficiency (en) 低纖維蛋白原血症 (zh)
name	Déficit congénital en fibrinogène (fr) Factor I Deficiency (en) 低纖維蛋白原血症 (zh)
instance of	wds:Q18354630-B941EE1A-A046-45B3-B5D0-D68A7AE7A168
instance of	class of disease
subclass of	wds:Q18354630-106FAF28-5C33-4924-8D09-5381DC3DF6F7 wds:Q18354630-7ED3FFFC-5908-4BFE-BAE0-6DCF38CE322A wds:Q18354630-9C3CF20F-9D00-4B53-B39A-F2DA9DF4083E
subclass of	fibrinogen abnormality inherited blood coagulation disease immunodeficiency due to a complement regulatory deficiency
Orphanet ID	wds:Q18354630-FB2A6236-B78E-452C-8CC2-C0FDA565A5A6
genetic association	wds:Q18354630-8D748451-3B18-4370-8902-5AD2D95CDAB9 wds:Q18354630-AEE66BB2-9BCF-4E0D-A749-29F5851AEB34 wds:Q18354630-C10F8E26-F92E-47F5-B81D-71F9977A183B
ICD-10-CM	wds:Q18354630-48D0C99C-B004-4863-B25D-A0AB13CB271A
GARD rare disease ID	wds:Q18354630-9C8D0904-9E57-4D80-BD88-1893EAE59B73
Orphanet ID	335
genetic association	FGA FGG FGB
ICD-10-CM	D68.2
GARD rare disease ID	2320
skos:altLabel	Fibrinogen deficiency, congenital (en) Hereditary deficiency of factor 1 (en) Hereditary deficiency of factor I (en) congenital fibrinogen deficiency (en)
OpenAlex ID	wds:Q18354630-BAA24A47-C1E1-4C25-A84E-33F9D2BAE3C5
UMLS CUI	wds:Q18354630-A4FA32C5-F747-4BE1-9E65-6BCA8D5BE0BF
ICD-11 ID (MMS)	wds:Q18354630-D65F8A2F-B6F9-4FD6-A244-00B6515425FA
ICD-11 (foundation)	wds:Q18354630-0D9821DE-8503-427F-AA8A-2455C460A1F1
OpenAlex ID	C2910129229
UMLS CUI	C2062367
ICD-11 ID (MMS)	3B14.0
ICD-11 (foundation)	1452989457
is owl:sameAs of	Factor I Deficiency
is about of	Factor I Deficiency https://www.wikidata.org/wiki/Special:EntityData/Q18354630 Factor I deficiency
is subclass of of	Congenital hypofibrinogenemia hypodysfibrinogenemia congenital afibrinogenemia
is subclass of of	wds:Q42417349-d2483a76-43c2-0661-3cd4-c0cc8961b279 wds:Q42417401-fb933c45-45d9-cf1d-0f14-8700a8fd4fc8 wds:Q5160407-e50a9c33-4f47-c598-5c06-f18eb063a7df
is main subject of	Efficacy and tolerability of a pasteurised human fibrinogen concentrate in patients with congenital fibrinogen deficiency Results of an international, multicentre pharmacokinetic trial in congenital fibrinogen deficiency Efficacy and safety of a new human fibrinogen concentrate in patients with congenital fibrinogen deficiency: an interim analysis of a Phase III trial. Efficacy and safety of fibrinogen concentrate for on-demand treatment of bleeding and surgical prophylaxis in paediatric patients with congenital fibrinogen deficiency Fibrinogen concentrate for treatment of bleeding and surgical prophylaxis in congenital fibrinogen deficiency patients Liquid Extradural Hematoma With Congenital Fibrinogen Deficiency, Case Report Function and behavior of thrombocytes in congenital fibrinogen deficiency Clinical pharmacology, efficacy and safety study of a triple-secured fibrinogen concentrate in adults and adolescent patients with congenital fibrinogen deficiency Fibrinogen concentrate for bleeding in patients with congenital fibrinogen deficiency: Observational study of efficacy and safety for prophylaxis and treatment Two-Pronged Treatment of Hemoperitoneum and Abnormal Uterine Bleeding in an Adolescent Girl With Congenital Fibrinogen Deficiency
is main subject of	wds:Q47384528-0108C9FB-9EF8-4473-8C16-8CE28E8B8D58 wds:Q104484007-CDA472C0-EBCA-4CA4-A184-9C5BA3E0A3DC wds:Q82680493-EFC35D03-5A67-4FFC-8F2A-563194212EEE wds:Q92305669-C9FAA272-18C0-4323-8177-52C329A047FE wds:Q69633459-A03DDDA3-8FD2-4E25-A728-D4CF69DDF8A0 wds:Q72200599-F071737A-D3A0-4E43-AF3C-1215CB167CCE wds:Q104464138-74F12982-25CB-41AA-9200-16295803150C wds:Q81789542-4EE79247-0D84-493E-A397-DCCE0A9F5F5C wds:Q96174298-234C370D-E8EC-4BC2-AC11-0E3C0B8DC247 wds:Q91127245-D96CD398-AAA0-4CD9-BF0C-A670D1FFDEE8
is genetic association of	FGA FGG CFI FGB
is genetic association of	wds:Q5446444-514F4255-5B35-4222-A9ED-9E419C770C3D wds:Q17928227-EC989FBC-36BE-48C5-B8E1-0CEA64D3A9C1 wds:Q5446445-0F03B35C-4B8E-4064-9DAA-0090C10F7936 wds:Q20970075-44F48BC7-39E6-49E7-9036-DE0D245FCF09

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