About: familial cold autoinflammatory syndrome 3

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

human disease

Attributes	Values
rdf:type	Item
owl:sameAs	familial cold autoinflammatory syndrome 3
description	human disease (en) մարդու հիվանդություն (hy) хвороба людини (uk)
exact match	wds:Q30989792-0825E895-1E8C-42BB-9273-F4CC9EE2E00E wds:Q30989792-58556FAD-B435-4891-B169-1B04773221D0
exact match	http://identifiers.org/doid/DOID:0090064 http://purl.obolibrary.org/obo/DOID_0090064
health specialty	wds:Q30989792-A2DDD53C-11B4-45C2-BE66-FE895D9DAAC5
Mondo ID	wds:Q30989792-5A49B083-F270-4354-8A1A-D591CB7D531D
Disease Ontology ID	wds:Q30989792-E14E148E-5ED6-43AB-AE47-FD8E17681999
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0013766
Disease Ontology ID	http://purl.obolibrary.org/obo/DOID_DOID:0090064
health specialty	dermatology
Mondo ID	MONDO_0013766
Disease Ontology ID	DOID:0090064
rdfs:label	syndrome familial autoinflammatoire au froid type 3 (fr) familial cold autoinflammatory syndrome 3 (en)
skos:prefLabel	syndrome familial autoinflammatoire au froid type 3 (fr) familial cold autoinflammatory syndrome 3 (en)
name	syndrome familial autoinflammatoire au froid type 3 (fr) familial cold autoinflammatory syndrome 3 (en)
instance of	wds:Q30989792-5C554244-4D32-41D7-A5E0-84593620F755 wds:Q30989792-FB763B4B-A908-4AFD-9826-71A94A2ADF04
instance of	class of disease rare disease
subclass of	wds:Q30989792-180F9D3E-A13E-4B4B-B742-526E39046F54 wds:Q30989792-63A61B44-A2AE-42CE-B95B-DDACB78CD1A8 wds:Q30989792-6EFC1585-10BB-4742-AE6B-A03C54303497 wds:Q30989792-8B3AE26E-C70E-459C-8388-666CF1249DE4 wds:Q30989792-d9efa5d0-4fae-18b5-93d4-b88ca4e3fde9
subclass of	Muckle-Wells syndrome skin disease autosomal dominant disease autoimmune connective tissue disorder autoimmune urticaria
Google Knowledge Graph ID	wds:Q30989792-33AE72FB-08C1-4A6E-936F-828B1FC1D58D
Google Knowledge Graph ID	http://g.co/kg/g/11hb69dbrk
Google Knowledge Graph ID	/g/11hb69dbrk
UniProt disease ID	wds:Q30989792-a39a1b85-4f4b-bbad-7a5b-c997032d8fad
Orphanet ID	wds:Q30989792-8AFDEA34-CBD6-4C3C-8B72-157342FDE3E5
genetic association	wds:Q30989792-3DA0449D-2B21-46D9-B9D3-FA53972129E7
ICD-10-CM	wds:Q30989792-663AF049-A060-4411-8DAD-578DAC7CCB1B
OMIM ID	wds:Q30989792-1D2ED6F4-AD9F-4E90-B8E4-251E624BFC5E
Genetics Home Reference Conditions ID	wds:Q30989792-D69B0911-75B1-469F-AFB5-77DCFCFC6AFD
UniProt disease ID	DI-03380
Orphanet ID	300359
genetic association	PLCG2
ICD-10-CM	L50.2
OMIM ID	614468
Genetics Home Reference Conditions ID	plcg2-associated-antibody-deficiency-and-immune-dysregulation
skos:altLabel	FCAS3 (en) PLAID (en) Antibody Deficiency and Immune Dysregulation, Plcg2-Associated (en) FACU (en) FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3 (en) FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3; FCAS3 (en) Familial Atypical Cold Urticaria (en) PLAID syndrome (en) familial cold autoinflammatory syndrome type 3 (en) PLCG2-associated antibody deficiency and immune dysregulation (en) Familial cold urticaria with common variable immunodeficiency (en)
UMLS CUI	wds:Q30989792-1C9BC381-C30D-41CD-92AD-2A5BD5CD6B75 wds:Q30989792-4088CE5B-842C-4037-AAFA-0C979DA1D335
on focus list of Wikimedia project	wds:Q30989792-DDCCAEAB-9D01-47D5-A0C7-C13D3D71FA09
UMLS CUI	C3280914 C4722480
on focus list of Wikimedia project	WikiProject Medicine
is owl:sameAs of	familial cold autoinflammatory syndrome 3
is about of	familial cold autoinflammatory syndrome 3 https://www.wikidata.org/wiki/Special:EntityData/Q30989792 PLAID syndrome
is main subject of	Plaid perception is only subtly impaired in strabismic amblyopia Synchronization dynamics in response to plaid stimuli in monkey V1. Interaction between binocular rivalry and depth in plaid patterns Plaid motion rivalry: correlates with binocular rivalry and positive mood state Familial atypical cold urticaria: description of a new hereditary disease Orientation processing mechanisms revealed by the plaid tilt illusion Biclustering with Flexible Plaid Models to Unravel Interactions between Biological Processes Perceived duration of plaid motion increases with pattern speed rather than component speed Depth-coded motion signals in plaid perception and optokinetic nystagmus Use of plaid patterns to distinguish the corticofugal and direct retinal inputs to the brainstem optokinetic nystagmus generator. Dependence of plaid motion coherence on component grating directions. Illusory position shift induced by plaid motion The oblique plaid effect. The barberplaid illusion: plaid motion is biased by elongated apertures. Two-dimensional tilt illusions induced by orthogonal plaid patterns: effects of plaid motion, orientation, spatial separation, and spatial frequency. Vernier acuity with plaid masks: the role of oriented filters in vernier acuity. Further evidence for monocular determinants of perceived plaid direction. Monocular mechanisms determine plaid motion coherence A role for a low level mechanism in determining plaid coherence. Plaid slant and inclination thresholds can be predicted from components. Cross-domain adaptation reveals that a common mechanism computes stereoscopic (cyclopean) and luminance plaid motion Anomalous perception of coherence and transparency in moving plaid patterns. Grating and plaid masks indicate linear summation in a contrast gain pool Grating and plaid chrominance motion influences the suppressed ocular following response Directional responses of visual wulst neurones to grating and plaid patterns in the awake owl Luminance contrast affects motion coherency in plaid patterns by acting as a depth-from-occlusion cue. PLAID: a Syndrome of Complex Patterns of Disease and Unique Phenotypes

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