Web Analysis for Rare-E-Connect - rare-e-connect.eu

2.50 Rating by CuteStat

It is a domain having eu extension. This website is estimated worth of $ 8.95 and have a daily income of around $ 0.15. As no active threats were reported recently by users, rare-e-connect.eu is SAFE to browse.

PageSpeed Score
0
Siteadvisor Rating
Not Applicable

Traffic Report

Daily Unique Visitors: Not Applicable
Daily Pageviews: Not Applicable

Estimated Valuation

Income Per Day: $ 0.15
Estimated Worth: $ 8.95

Search Engine Indexes

Google Indexed Pages: Not Applicable
Bing Indexed Pages: Not Applicable

Search Engine Backlinks

Google Backlinks: Not Applicable
Bing Backlinks: Not Applicable

Safety Information

Google Safe Browsing: No Risk Issues
Siteadvisor Rating: Not Applicable
WOT Trustworthiness: Not Applicable
WOT Child Safety: Not Applicable

Website Ranks & Scores

Alexa Rank: Not Applicable
Domain Authority: Not Applicable

Web Server Information

Hosted IP Address:

35.214.234.137

Hosted Country:

The Netherlands NL

Location Latitude:

53.2157

Location Longitude:

6.5765
Page Title of rare-e-connect.eu
RARE-e-CONNECT - RARE-e-CONNECT
Meta Keywords of rare-e-connect.eu
clinical trials, cancer, networking, file sharing, webinars, fibromyalgia, publications, specialists, anorexia nervosa, online communities, cystic fibrosis, down syndrome, fsh, rett syndrome, ehlers danlos syndrome, medical resources, rare diseases, clinical guidelines, becker, muscular dystrophy, hydrocephalus, aplastic anemia, myasthenia gravis, trigeminal neuralgia, uterine fibroids, wolf hirschhorn syndrome, pectus excavatum, marfan syndrome, retinitis pigmentosa, hidradenitis suppurativa, lymphedema, noonan syndrome, turner syndrome, fabry's disease, retinoblastoma, educational material, patient advice, parkinsons, idiopathic pulmonary fibrosis, dwarfism, familial mediterranean fever, thalassaemia, albinism, epidermolysis bullosa, lupus erythematosus, mastocytosis, pemphigus, tuberous sclerosis, familial adenomatous polyposis, interstitial cystitis, primary immunodeficiency, primary sclerosing cholangitis, bone cancer, multidisciplinary teams, angelman syndrome, patient stories, phenylketonuria, fibrous dysplasia, wilson disease, fragile x syndrome, klinefelter syndrome, gaucher disease, ichthyosis vulgaris, duchenne muscular dystrophy, brugada syndrome, rare disorders, neutropenia, cholesteatoma, myopathy, williams syndrome, haemophilia, familial cold urticaria, paget disease, alstrom syndrome, crouzon syndrome, apert syndrome, professional communities, cystinosis, myotonic dystrophy, lipodystrophy, huntington's disease, hereditary angioedema, behcet disease, metopic craniosynostosis, achondroplasia, aplastic anaemia, continuous medical education, mowat-wilson syndrome, addisons disease, pompe disease, multidisciplinary care, guillain barre, ollier disease, patau syndrome, polyarteritis nodosa, no diagnosis, healthcare collaboration, dumping syndrome, spinal muscular atrophy type ii, medical communities, familial chylomicronemia syndrome, medical teams, patient communities, metastatic colon cancer, cornelia de lange syndrome, sotos, fructosaemia, relapsing polychondritis, acrodysostosis, dravet syndrome, dyrk1a, e-learning, information rare diseases, patient collaboration, rare disease specialist, medical collaboration cyprus, rare disease collaboration, medical collaboration, healthcare teams, medical decision making support, multidisciplinary rare disease care, specialist centres, specialisation rare diseases, european reference networks, recurrent cold urticaria and angioedema, kienbock's disease, russell-silver syndrome, short stature syndromes, xlh (x-linked hypophosphatemia), osteoarthritis/rheumatoid arthritis, chronic recurrent multifocal osteomyelitis (crmo), coarctation of the aorta/ebstein anomaly, pachygyria, arteriovenous malformation- avs, hirschsprung disease, addison’s disease, cushing disease, pituary deficiency, von willebrand haemophilia/systemic lupus erythematosus (sle), pituitary microadenoma (cushing syndrome), myeloid cancer with pheochromocytoma, norrie disease, chron’s disease, colon atresia, barret oesophagus, cri du chat syndrome, macula lutea/ marfan syndrome/ adams syndrome, stickler syndrome, oculo-dento-digital, mosaicism/ lethal genes, smith magenis syndrome, olmsted syndrome, benign chronic familial pemphigus of hailey-hailey, acute aortic dissection type b, chronic pelvic pain - vulvodynia, extrapelvic endometriosis, c1 inhibitor defieciency hereditary angioderma, thalassaemia/severe myelofibrosis and agnogenic myeloid metaplasia, non hodgkin`s lymphoma, langerhans cell hystiocytosis, idiopathic angioedema type i, skin mastocytosis, ascites - budd chiari syndrome/ behcet syndrome, hepatocellular cancinoma, syndrome caroli, familial amyloid polyneuropathy, familial amyloidosis, ethylmalonic encephalopathy, galactosaemia, gm1 gangliosidosis type 1, hereditary metabolic disease, methylmalonic acidemia, sandhoff disease, tay-sachs disease, lstrom syndrome, paraneoplastic syndrome/ ovary cancer/ endometrium cancer, tuberous sclerosis- symptomatic focal epilepsy, amyotrophic lateral sclerosis - als, chronic inflammatory demyelinating polyneuropathy (cidp), complex regional pain syndrome (crps) type ii, devic syndrome, friedreich`s ataxia, gangliosidosis gm1, guillain–barré syndrome (gbs), meige syndrome, mitochondrial encephalopathy, lactic-acidosis and stroke-like episodes (melas), multiple system atrophy - msa or shy–drager syndrome, neurodegeneration with brain iron accumulation 5 (nbia5), neurofibromatosis type i, neurofibromatosis type ii, romberg syndrome, spinal muscular atrophy type i, spinal muscular atrophy type iii, spinocerebellar ataxia (sca ), foix alajouanine, parry romberg, primary erythromelalgia, ring chromosome 14 syndrome, retinitis pigmentosa - nephropathy gene cfhr5, refractory schizophrenia, methylmalonic encephalopathy, sinking-skin-flap-syndrome, glioma iv in spinal cord, als (amyotrophic lateral sclerosis), limb girdle muscular dystrophy (lgmd2a), mnd (motor neurone disease), werdnig-hoffmann disease, charcot-marie-tooth(cmt), myalgic enchephalomyelitis or chronic fatigue syndrome, periodic cyclic vomiting, fisher miller syndrome/ bickerstaff encephalitis, neurological- no diagnosis, chronic immunodeficiency, common variable immunodeficiency (cvid), cvid billu, kartagener syndrome, lymphangioleiomyomatosis (lam) disease/ tuberous sclerosis, primary ciliary dyskinesia (pcd), pyle disease, (goldenhar syndrome)/ oculo-auriculo-vertebral (oav) syndrome), joubert syndrome/ oral-facial-digital syndrome type 6, pten syndrome, microduplication 16p11.2, achalasia of oesophagus, gitelman syndrome, acute intermittent porphyria, igg4 related disease / liver cirrhosis, acquired angioedema, bartter syndrome, muc1 kidney disease, renal tubular acidosis (rta), pseudo-bartter syndrome, takayasu arteritis, rheumatopathy, post traumatic arthritis, adamantiades-behcet's disease (abd)/ fibromyalgia, stevens-johnson syndrome, erdheim-chester disease, acute multifocal myelitis, alagille syndrome

Page Resources Breakdown

Homepage Links Analysis

Website Inpage Analysis

H1 Headings: Not Applicable H2 Headings: 3
H3 Headings: 8 H4 Headings: Not Applicable
H5 Headings: Not Applicable H6 Headings: Not Applicable
Total IFRAMEs: 1 Total Images: 20
Google Adsense: Not Applicable Google Analytics: UA-156924051-1

Websites Hosted on Same IP (i.e. 35.214.234.137)

altrove • I am somewhere else
- iosonoaltrove.com
Not Applicable $ 8.94

HTTP Header Analysis

HTTP/2 200
server: nginx
date: Mon, 25 Mar 2024 03:24:21 GMT
content-type: text/html; charset=utf-8
vary: Accept-Encoding
expires: Wed, 17 Aug 2005 00:00:00 GMT
cache-control: no-store, no-cache, must-revalidate, post-check=0, pre-check=0
pragma: no-cache
x-content-type-options: nosniff
last-modified: Mon, 25 Mar 2024 03:24:21 GMT
x-httpd: 1
host-header: 6b7412fb82ca5edfd0917e3957f05d89
x-proxy-cache: MISS
x-proxy-cache-info: 0 NC:000000 UP:SKIP_CACHE_SET_COOKIE
content-encoding: br

Domain Information

Domain Registrar: Registrar.eu

Domain Nameserver Information

Host IP Address Country
ns1.siteground.net 75.2.77.104 United States of America United States of America
ns2.siteground.net 99.83.229.113 United States of America United States of America

Full WHOIS Lookup

% The WHOIS service offered by EURid and the access to the records
% in the EURid WHOIS database are provided for information purposes
% only. It allows persons to check whether a specific domain name
% is still available or not and to obtain information related to
% the registration records of existing domain names.
%
% EURid cannot, under any circumstances, be held liable in case the
% stored information would prove to be wrong, incomplete or not
% accurate in any sense.
%
% By submitting a query you agree not to use the information made
% available to:
%
% - allow, enable or otherwise support the transmission of unsolicited,
% commercial advertising or other solicitations whether via email or
% otherwise;
% - target advertising in any possible way;
%
% - to cause nuisance in any possible way to the registrants by sending
% (whether by automated, electronic processes capable of enabling
% high volumes or other possible means) messages to them.
%
% Without prejudice to the above, it is explicitly forbidden to extract,
% copy and/or use or re-utilise in any form and by any means
% (electronically or not) the whole or a quantitatively or qualitatively
% substantial part of the contents of the WHOIS database without prior
% and explicit permission by EURid, nor in any attempt hereof, to apply
% automated, electronic processes to EURid (or its systems).
%
% You agree that any reproduction and/or transmission of data for
% commercial purposes will always be considered as the extraction of a
% substantial part of the content of the WHOIS database.
%
% By submitting the query you agree to abide by this policy and accept
% that EURid can take measures to limit the use of its WHOIS services
% in order to protect the privacy of its registrants or the integrity
% of the database.
%
% The EURid WHOIS service on port 43 (textual whois) never
% discloses any information concerning the registrant.
% Registrant and on-site contact information can be obtained through use of the
% webbased WHOIS service available from the EURid website www.eurid.eu
%
% WHOIS rare-e-connect.eu
Domain: rare-e-connect.eu
Script: LATIN

Registrant:
NOT DISCLOSED!
Visit www.eurid.eu for webbased WHOIS.

On-site(s):
NOT DISCLOSED!
Visit www.eurid.eu for webbased WHOIS.

Registrar:
Name: Registrar.eu
Website: https://www.openprovider.com

Name servers:
ns2.siteground.net
ns1.siteground.net

Please visit www.eurid.eu for more info.
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