Malaltiesminoritaries.org SEO Analysis

Pagespeed Score
Desktop 25/100
Mobile 17/100
Optimization Stats
Field Data Result
Page Size 57 KB
Compression NO
Text/Html Ratio 4144 / 58799 (bytes) = 7.05%
Load Time 0.69 second
Mobile Ready 0/100
In-Page Links 68
Doc Type HTML 5
Encoding UTF-8
Declared Language English
Preferred Domain No
Robots.txt No
Url Rewrite Yes
Underscores in url Yes
Images Without ALT 10 / 28
Embedded Objects (Desktop) No
Embedded Objects (Mobile) Yes
Iframe Yes
Custom 404 page Yes
Email Privacy Yes
Gsafe browsing Yes
Analytics Yes
W3C Validity No
Keyword Consistency
Keywords Freq Title Desc <H>
febrer 14
malalties 8
summer 4
jornada 3
mundial 3
d'aquesta 2
medicamentos 2
tindrÀlloc 2
barcelona 2
juny 2
minoritÀries 2
motiu 2
marÇ 2
edició 2
llegir 2
36/100
Update

September, 25 2023

With 0.69 seconds in page load, 57 KB of page size and all other reports below, the malaltiesminoritaries.org has a SEO score of 36 out of 100

Meta tags data
Title Malalties Minoritàries-
Description Unitat funcional Plataforma Malalties Minoritàries de l’Institut Català de la Salut, que té com a objectiu principal la millorar de l’accés a la informació i formació, la cura i recolzament a les persones que viuen afectades per una malaltia crònica, complexa, vulnerable o minoritària.
Keyword associacions, associació, malaltia minoritària, malaltia de baixa prevalença, junts fem pinya, pacient expert, pacient empoderat, plataforma malalties minoritàries, dia mundial malalties minoritàries, summer school spanish edition, afectats, afectada, afectat, designació medicaments orfes, salut, cromosòmica, comitè d’ètica, ERN, XUEC, renals, respiratòries, sistema immunitari, lisosomal, malformació congènita, hepàtiques, metabòlica, neonatal, neoplàsia, oncologia, trastorn cognitiu, trastorn del comportament, trastorn sensorial, neurodegenerativa, teràpia gènica, mutació genètica, malaltia hereditària, malaltia de novo, formació, designación medicamentos huérfanos, rare disease day, enfermedades poco frecuentes, enfermedades raras, 22q11, digeorge, vcfs, amaurosis congènita de leber, anèmia de fanconi, angelman, anirídia, apert, artrogriposis múltiple congènita, asperger, atàxies hereditàries, atresia d’esòfag, atrofia muscular espinal, atrofia vesical, behçet, biliars inflamatòries, brown vialetto van laere, brugada, càncer, cardiopaties congènites, cardiopaties infantils, chiari, cistinosis, cistitis intersticial, cornelia de lange, dèficit de alfa 1, dèficit de lipasa àcida lisosomal, dèficits immunitaris primaris, dèficits immunitaris primaris, dent, displàsia ectodèrmica, distonia, distròfia muscular congènita per dèficit de col·lagen vi, distròfia muscular de cintures per dèficit de sarcoglicanos, dravet, duchenne, becker, duplicació mecp2, ehlers-danlos e hiperlaxitut, epilèpsia, esclerodèrmia, esclerosi lateral amiotròfica, esclerosi tuberosa, esclerosis múltiple espina bífida i hidrocefàlia, fabry, fatiga crònica, encefalomielitits miàlgica, fibrosi quística, síndromes autoinflamatoris, galactosèmia, gaucher , glucogenosis, glut1, hemiplejia alternante, hemocromatosis, hemofília, hemoglobinúria paroxística nocturna, hemolitico urenico atopico, hernia diafragmàtica congènita, hiperplàsia suprarenal congènita, hipertensió pulmonar, hipertensió pulmonar, hipomagnesemia familiar, huntington, ictiosis, koolen-de vries, lesch-nyhan, leucèmia, lisosomals, lupus , lyme, macrocefàlia con malformació capil·lar, marfan, mastocitosis, miasténico congènit, miopatia miotubular y centronuclear, neuroblastoma, neurofibromatosis, neuromusculars, niemann pick, opitz c, osteogènesis imperfecta, paraparesia espàstica familiar, phelan-mcdermid, pell de papallona debra, crisper, diversitat funcional, teràpies avançades, accés al medicament, epigenètica, exposoma, pku-atm, prader willi, raquitisme, retinosi pigmentària, rett, rubistein-taybi, sanfilippo, siringomièlia, sjögren, stargardt go, stickler, tics , síndrome de tourette, síndrome de turner, von hippel lindau, síndrome de west, síndrome de williams, x fràgil, xantomatosis cerebrotendinosa, distrofia muscular congènita per dèficit de Merosina DMC1A-LAMA2, ema, eurordis, fundació institut de recerca sant pau, uab, fundació doctor robert, comp, ics, departament de salut, comitè organitzador dia mundial de les malalties minoritàries, aemps, ciberer, direcció hospitals ics
Domain Registration
Age 9 Years, 344 Days
Created 15th-Oct-2013
Updated 29th-Nov-2022
Expiry 15th-Oct-2023
DNS Data
Host Type Ttl Other
malaltiesminoritaries.org A 3593 ip:151.236.39.40
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http Headers
HTTP/1.1 302 Object moved
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Date: Sun, 24 Sep 2023 23:08:04 GMT
Content-Length: 140

HTTP/1.1 200 OK
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WHOIS Data
Domain Name: malaltiesminoritaries.org
Registry Domain ID: c21a553d52ec41fdbe71300a53bbf2b0-LROR
Registrar WHOIS Server: http://whois.nicline.com
Registrar URL: http://nicline.com/whois/whois.htm
Updated Date: 2022-11-29T15:53:42Z
Creation Date: 2013-10-15T15:53:15Z
Registry Expiry Date: 2023-10-15T15:53:15Z
Registrar: Arsys Internet, S.L. dba NICLINE.COM
Registrar IANA ID: 379
Registrar Abuse Contact Email: domainnames@arsys.es
Registrar Abuse Contact Phone: +34.941620100
Domain Status: ok https://icann.org/epp#ok
Registry Registrant ID: REDACTED FOR PRIVACY
Registrant Name: REDACTED FOR PRIVACY
Registrant Organization: NULL
Registrant Street: REDACTED FOR PRIVACY
Registrant City: REDACTED FOR PRIVACY
Registrant State/Province: BARCELONA
Registrant Postal Code: REDACTED FOR PRIVACY
Registrant Country: ES
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Registrant Fax Ext: REDACTED FOR PRIVACY
Registrant Email: Please query the RDDS service of the Registrar of Record identified in this output for information on how to contact the Registrant, Admin, or Tech contact of the queried domain name.
Registry Admin ID: REDACTED FOR PRIVACY
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Admin Email: Please query the RDDS service of the Registrar of Record identified in this output for information on how to contact the Registrant, Admin, or Tech contact of the queried domain name.
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Tech Email: Please query the RDDS service of the Registrar of Record identified in this output for information on how to contact the Registrant, Admin, or Tech contact of the queried domain name.
Name Server: ns10.piensasolutions.com
Name Server: ns9.piensasolutions.com
DNSSEC: unsigned
URL of the ICANN Whois Inaccuracy Complaint Form: https://www.icann.org/wicf/
>>> Last update of WHOIS database: 2023-09-24T23:08:07Z
Server Location
Server IP 151.236.39.40
Server Location United Kingdom
Service Provider Simply Transit Ltd
Domain Availability
Domains (TLD) Status
malaltiesminoritaries.com Available
malaltiesminoritaries.net Available
malaltiesminoritaries.biz Available
malaltiesminoritaries.io Already Registered
malaltiesminoritaries.info Already Registered
Typo Availability
Domains (TLD) Status
nalaltiesminoritaries.org Already Registered
halaltiesminoritaries.org Already Registered
jalaltiesminoritaries.org Already Registered
kalaltiesminoritaries.org Already Registered
lalaltiesminoritaries.org Already Registered
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