congenital afibrinogenemia (Q5160407): Preview

congenital afibrinogenemia (Q5160407)
Human disease

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Current Data About congenital afibrinogenemia

(P31)

(Q112193867)

(P279)

(Q18354630)

(Q18555031)

(P248)
(P813)	Wednesday, May 15, 2019
(P699)	DOID:2236

(Q10267817)

(P248)
(P813)	Sunday, November 29, 2020
(P699)	DOID:2236

(Q890200)

(P248)
(P813)	Sunday, November 29, 2020
(P699)	DOID:2236

(P1709)

http://purl.obolibrary.org/obo/DOID_0050878

(P248)
(P813)	Thursday, February 4, 2016
(P1065)	https://raw.githubusercontent.com/DiseaseOntology/HumanDiseaseOntology/9b96f2e36e01ad4cf87c5cef1ac0c2e8708157d6/src/ontology/doid.owl

http://identifiers.org/doid/DOID:0050878

(P854)	http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233

(P1748)

C98130

(P248)
(P813)	Wednesday, May 15, 2019
(P699)	DOID:2236

(P1995)

(Q103824)

(P2293)

(Q17928227)

(P248)
(P813)	Thursday, August 24, 2023
(P854)	https://platform.opentargets.org/evidence/ENSG00000171557/Orphanet_98880
(P887)

(Q5446445)

(P248)
(P813)	Thursday, August 24, 2023
(P854)	https://platform.opentargets.org/evidence/ENSG00000171564/Orphanet_98880
(P887)

(P2888)

http://purl.obolibrary.org/obo/DOID_2236

(P248)
(P813)	Sunday, November 29, 2020
(P699)	DOID:2236

http://identifiers.org/doid/DOID:2236

(P248)
(P854)	https://registry.identifiers.org/registry/doid

http://purl.obolibrary.org/obo/DOID_0050878

(P248)
(P813)	Monday, November 30, 2020
(P699)	DOID:0050878

http://identifiers.org/doid/DOID:0050878

(P248)
(P854)	https://registry.identifiers.org/registry/doid

(P5008)

(Q4099686)

other details

aliases	Factor I deficiency Fibrinogen deficiency Afibrinogenemia CAFBN
description	Human disease

External Links

(P486)	D000347
(P492)	202400
(P493)	286.3
(P557)	307
(P604)	001313
(P665)	H00222
(P672)	C15.378.100.100.056 C15.378.100.141.072 C15.378.463.067 C16.320.099.056
(P699)	DOID:2236 DOID:0050878
(P1417)	science/afibrinogenemia
(P1550)	98880
(P2581)	00021809n
(P2892)	C0001733
(P3827)	afibrinogenemia
(P4233)	congenital-afibrinogenemia
(P4317)	5761
(P4746)	019842
(P5270)	MONDO_0008737
(P6366)	2776926982
(P7464)	congenital-afibrinogenemia
(P10283)	C2910029113
(P11143)	Congenital afibrinogenemia
(P11430)	DI-01387