MCID: INT182
MIFTS: 20

Intermittent Hydrarthrosis

Categories: Bone diseases, Rare diseases

Aliases & Classifications for Intermittent Hydrarthrosis

MalaCards integrated aliases for Intermittent Hydrarthrosis:

Name: Intermittent Hydrarthrosis 59
Intermittent Joint Effusion 73

Classifications:



External Ids:

Orphanet 59 ORPHA329967
ICD10 via Orphanet 34 M12.4
ICD10 33 M12.4
UMLS 73 C0149910

Summaries for Intermittent Hydrarthrosis

MalaCards based summary : Intermittent Hydrarthrosis, also known as intermittent joint effusion, is related to hydrarthrosis and synovitis. An important gene associated with Intermittent Hydrarthrosis is MEFV (MEFV, Pyrin Innate Immunity Regulator), and among its related pathways/superpathways is Toll-like Receptor Signaling Pathway. Affiliated tissues include bone.

Wikipedia : 76 Intermittent hydrarthrosis (IH), also known as periodic synoviosis, periodic benign synovitis, or... more...

Related Diseases for Intermittent Hydrarthrosis

Graphical network of the top 20 diseases related to Intermittent Hydrarthrosis:



Diseases related to Intermittent Hydrarthrosis

Symptoms & Phenotypes for Intermittent Hydrarthrosis

Drugs & Therapeutics for Intermittent Hydrarthrosis

Search Clinical Trials , NIH Clinical Center for Intermittent Hydrarthrosis

Genetic Tests for Intermittent Hydrarthrosis

Anatomical Context for Intermittent Hydrarthrosis

MalaCards organs/tissues related to Intermittent Hydrarthrosis:

41
Bone

Publications for Intermittent Hydrarthrosis

Articles related to Intermittent Hydrarthrosis:

(show all 17)
# Title Authors Year
1
Successful Treatment of Intermittent Hydrarthrosis With Hydroxychloroquine. ( 26587859 )
2015
2
Anakinra for a refractory case of intermittent hydrarthrosis with a TRAPS-related gene mutation. ( 22887853 )
2013
3
May some cases of intermittent hydrarthrosis represent an atypical form of calcium pyrophosphate dihydrate crystal deposition disease? Usefulness of mutational analysis of the MEFV gene. ( 17889261 )
2008
4
Association of intermittent hydrarthrosis with MEFV gene mutations. ( 16802374 )
2006
5
Successful therapy with low-dose colchicine in intermittent hydrarthrosis. ( 12595650 )
2003
6
Intermittent hydrarthrosis. ( 11273267 )
1998
7
Participation of synovial mast cells in intermittent hydrarthrosis. ( 2467680 )
1989
8
Calcium pyrophosphate crystals in intermittent hydrarthrosis. ( 3029370 )
1986
9
LE cells in intermittent hydrarthrosis. ( 6157396 )
1980
10
Periodic synoviosis (intermittent hydrarthrosis) with observations and studies on a patient. ( 4464498 )
1974
11
Intermittent hydrarthrosis; periodic benign synovitis. ( 13567199 )
1958
12
Intermittent hydrarthrosis. ( 13383213 )
1957
13
Periodic benign synovitis; idiopathic intermittent hydrarthrosis. ( 13367081 )
1956
14
Intermittent hydrarthrosis. ( 14372871 )
1955
15
Intermittent hydrarthrosis. ( 14933539 )
1952
16
Intermittent hydrarthrosis; two cases. ( 15390577 )
1949
17
Intermittent Hydrarthrosis: (Hydrops Intermittens Articulorum). ( 21433466 )
1930

Variations for Intermittent Hydrarthrosis

Expression for Intermittent Hydrarthrosis

Search GEO for disease gene expression data for Intermittent Hydrarthrosis.

Pathways for Intermittent Hydrarthrosis

Pathways related to Intermittent Hydrarthrosis according to GeneCards Suite gene sharing:

# Super pathways Score Top Affiliating Genes
1
Show member pathways
11.48 MEFV TNFRSF1A

GO Terms for Intermittent Hydrarthrosis

Biological processes related to Intermittent Hydrarthrosis according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 inflammatory response GO:0006954 8.96 MEFV TNFRSF1A
2 negative regulation of inflammatory response GO:0050728 8.62 MEFV TNFRSF1A

Sources for Intermittent Hydrarthrosis

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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