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antithrombin III deficiency
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inherited blood coagulation disease characterized by the tendency to form clots in the veins
Attributes
Values
rdf:type
Item
owl:sameAs
antithrombin III deficiency
description
Krankheit
(de)
хвороба
(uk)
inherited blood coagulation disease characterized by the tendency to form clots in the veins
(en)
thrombophilie héréditaire qui augmente le risque de maladies thromboemboliques (thrombose veineuse profonde ou phlébite et embolie pulmonaire).
(fr)
rara patologia ereditaria. La trasmissione è generalmente autosomica dominante
(it)
exact match
wds:Q3704732-57E47CA4-A692-4637-B406-796BF34782B4
wds:Q3704732-81DC53E8-2583-4D49-B0E9-7BF3B63D5B66
wds:Q3704732-82E19876-EA7E-4485-B31F-A581DB4CAC7B
wds:Q3704732-EA6B8D5A-74BB-4D97-94A0-4DD7E1ADC46D
exact match
http://purl.obolibrary.org/obo/DOID_3755
http://purl.obolibrary.org/obo/HP_0001976
http://identifiers.org/doid/DOID:3755
http://www.orpha.net/ORDO/Orphanet_82
health specialty
wds:Q3704732-00E280DA-3547-4614-86D5-3B6774A4BB8B
Mondo ID
wds:Q3704732-D3DF6BBF-5D9D-425A-9D88-AE7041A97D40
DiseasesDB
wds:q3704732-FF2F6BAF-B04D-4F66-B24B-1A13B1B14DE5
Disease Ontology ID
wds:Q3704732-AE6938E1-22CB-484D-B600-099F6A100F55
Mondo ID
http://purl.obolibrary.org/obo/MONDO_0013144
Disease Ontology ID
http://purl.obolibrary.org/obo/DOID_DOID:3755
health specialty
hematology
Mondo ID
MONDO_0013144
DiseasesDB
783
Disease Ontology ID
DOID:3755
rdfs:label
antithrombin III deficiency
(en)
deficit di antitrombina III
(it)
deficiència d'antitrombina III
(ca)
deficiência de antitrombina III
(pt)
déficit en antithrombine III
(fr)
アンチトロンビン欠乏症
(ja)
skos:prefLabel
antithrombin III deficiency
(en)
deficit di antitrombina III
(it)
deficiència d'antitrombina III
(ca)
deficiência de antitrombina III
(pt)
déficit en antithrombine III
(fr)
アンチトロンビン欠乏症
(ja)
name
antithrombin III deficiency
(en)
deficit di antitrombina III
(it)
deficiència d'antitrombina III
(ca)
deficiência de antitrombina III
(pt)
déficit en antithrombine III
(fr)
アンチトロンビン欠乏症
(ja)
instance of
wds:Q3704732-258EA412-BD12-4A10-9F77-A0F095D0626E
wds:Q3704732-BEA63F85-1E82-44B8-B4C9-D3E6FB52FEDE
instance of
class of disease
rare disease
subclass of
wds:Q3704732-157D0F69-E3A5-4DF2-A8B0-CFBF9C72998C
wds:Q3704732-2F9C877A-3523-41AF-82C7-28C86C42734B
wds:Q3704732-B57FB9DC-F096-4195-9CB3-20E8F4844C55
wds:Q3704732-C976F567-75D8-47B9-B5FF-E0B992AB6B64
wds:Q3704732-D65613D7-A610-40AC-914B-5262D2C348C6
wds:Q3704732-FC0C8490-2801-4690-B3B3-D225DF1F2F0B
subclass of
thrombophilia
disease
autosomal recessive disease
autosomal dominant disease
inherited blood coagulation disease
hereditary thrombophilia
eMedicine ID
wds:q3704732-23AD4770-458C-4E51-91E1-78ECFE0809FF
eMedicine ID
954688
KEGG ID
wds:Q3704732-A73E1FC0-AAB4-417D-BDC9-DE6850D58AF7
KEGG ID
http://www.kegg.jp/entry/H01381
KEGG ID
H01381
UniProt disease ID
wds:Q3704732-49d3d19c-47d2-0f76-ed6c-abb28eb793d1
Orphanet ID
wds:Q3704732-0424DEB6-A81D-4ED4-B40C-1155F468C0B5
ICD-9-CM
wds:Q3704732-42E5064C-F1DF-48A7-99E8-37A8E91E8C3D
genetic association
wds:Q3704732-608AF2BF-FF7E-4BB7-A72E-E339081B3AA2
ICD-10-CM
wds:Q3704732-323DB6C3-1C4B-48B7-BF30-729168E09639
wds:Q3704732-DE37946C-3D90-4F68-9563-B05060506D85
PatientsLikeMe condition ID
wds:Q3704732-f6bceb7d-498e-b716-5ac6-e151e26ac467
GARD rare disease ID
wds:Q3704732-B9BF2C7A-3A96-423E-9D78-8D3E31930B6B
OMIM ID
wds:Q3704732-A01BCD19-E6D4-43F5-9F23-BE3734BBE769
UniProt disease ID
DI-00124
Orphanet ID
82
ICD-9-CM
286.9
genetic association
SERPINC1
ICD-10-CM
D68.59
D68.5
PatientsLikeMe condition ID
antithrombin-iii-deficiency
GARD rare disease ID
6148
OMIM ID
613118
Human Phenotype Ontology ID
wds:Q3704732-68B6B1F5-B5D2-45F4-89B4-1C07369F4127
Human Phenotype Ontology ID
HP:0001976
skos:altLabel
ANTITHROMBIN III DEFICIENCY
(en)
ANTITHROMBIN III DEFICIENCY; AT3D
(en)
AT III deficiency
(en)
AT3D
(en)
Deficit congenito di antitrombina
(it)
Deficit di antitrombina
(it)
Deficiência de antitrombina iii
(pt)
Thrombophilia Due to Antithrombin 3 Deficiency
(en)
hereditary thrombophilia due to congenital antithrombin deficiency
(en)
Hereditary thrombophilia due to congenital antithrombin 3 deficiency
(en)
OpenAlex ID
wds:Q3704732-DAA0A1B6-8077-4F54-B52C-A3386B325C35
NCI Thesaurus ID
wds:Q3704732-16BA845E-D96B-47CE-94CF-D8AD97E01334
UMLS CUI
wds:Q3704732-269228B1-399D-400F-B2A6-E7F7688672DF
wds:Q3704732-9697AEA0-4F4D-4655-A164-8A62503A62D9
MeSH descriptor ID
wds:Q3704732-7C8F262A-B3C8-4FEE-9544-46D4FD73FB40
on focus list of Wikimedia project
wds:Q3704732-791EDBFF-CDA4-49A7-AB80-47A92D5019DC
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