https://wevird.com 2026-07-25T08:21:29+00:00 always 0.5 https://freight.cargo.site/t/original/i/J2545067519164103851153392337191/square.svg Test 001 https://freight.cargo.site/t/original/i/C2843999978150976653176366148210/we-vird-logo.png Test 012 https://freight.cargo.site/t/original/i/A3019757192253540813363648899698/AA-copy.jpg Test 001 https://freight.cargo.site/t/original/i/K3019757192438008254100744415858/BB-copy.jpg Test 002 https://freight.cargo.site/t/original/i/W3019757192474901742248163519090/DD-copy.jpg Test 006 https://freight.cargo.site/t/original/i/F3019757192585582206690420828786/JJ-copy.jpg Test 011 https://freight.cargo.site/t/original/i/B3019757192511795230395582622322/FF-copy.jpg Test 007 https://freight.cargo.site/t/original/i/S3019757192530241974469292173938/GG-copy.jpg Test 008 https://freight.cargo.site/t/original/i/S3019757192548688718543001725554/HH-copy.jpg Test 009 https://freight.cargo.site/t/original/i/H3019757192567135462616711277170/II-copy.jpg Test 010 https://freight.cargo.site/t/original/i/N3019757192456454998174453967474/CCcopy.jpg Test 003 https://freight.cargo.site/t/original/i/N3019757192493348486321873070706/EE-copy.jpg Test 005 https://wevird.com/acalvaria 2026-07-27T12:33:27+00:00 always 0.5 https://freight.cargo.site/t/original/i/Q3018366521197658790065024248434/acalvaria.jpg https://freight.cargo.site/t/original/i/R3054511663454809122693506902642/ACALVARIA-b-1.jpg https://freight.cargo.site/t/original/i/I3054545224317278697281724852850/acalvaria-photo.jpg References 1. Orphanet. Acalvaria. <a href="https://www.orpha.net/en/disease/detail/945" target="_blank">https://www.orpha.net/en/disease/detail/945</a> 2. NIH Genetic and Rare Diseases Information Center (GARD). Acalvaria. 3. Harris CP, Townsend JJ, Carey JC. Acalvaria: A Unique Congenital Anomaly. American Journal of Medical Genetics. 1993;46(6):694–699. <a href="https://onlinelibrary.wiley.com/doi/10.1002/ajmg.1320460620" target="_blank">https://onlinelibrary.wiley.com/doi/10.1002/ajmg.1320460620</a> 4. Moore KR, Kapur RP, Siebert JR, et al. Acalvaria and Hydrocephalus: A Case Report and Discussion of the Literature. Journal of Ultrasound in Medicine. 1999. 5. Khadilkar VV, Khadilkar AV, Nimbalkar AA, Kinnare AS. Acalvaria. Indian Pediatrics. 2004. https://freight.cargo.site/t/original/i/U3054549637811478796734206290546/Acalvaria-Infographic-copy.jpg https://wevird.com/example-project-aip 2026-07-26T17:36:57+00:00 always 0.5 https://freight.cargo.site/t/original/i/U3018194343955501035758757063282/ig-copy.jpg https://freight.cargo.site/t/original/i/K3018237168367016057662186433138/wevb.jpg 1. GeneReviews®. Acute Intermittent Porphyria. 2. Orphanet. Acute Intermittent Porphyria. <a href="https://www.orpha.net/en/disease/detail/792" target="_blank">https://www.orpha.net/en/disease/detail/792</a> 3. American Porphyria Foundation. Acute Intermittent Porphyria (AIP). <a href="https://porphyriafoundation.org/for-patients/types-of-porphyria/aip/" target="_blank">https://porphyriafoundation.org/for-patients/types-of-porphyria/aip/</a> https://freight.cargo.site/t/original/i/S3051844858043995710166590270066/AIP-W.png https://wevird.com/example-project-loc 2026-07-26T11:09:53+00:00 always 0.5 https://freight.cargo.site/t/original/i/U3018194343955501035758757063282/ig-copy.jpg https://freight.cargo.site/t/original/i/P3018247443387932554619532061298/LOC-info-copy-WEB.jpg https://freight.cargo.site/t/original/i/D3052856418920585507949385329266/LOC-W.png https://freight.cargo.site/t/original/i/F3052858596429596200845986736754/LOC-1-copy2.jpg 1. Orphanet. Laryngo-onycho-cutaneous syndrome. <a href="https://www.orpha.net/en/disease/detail/69085" target="_blank">https://www.orpha.net/en/disease/detail/69085</a> 2. MedlinePlus Genetics. Laryngo-onycho-cutaneous syndrome. 3. GeneReviews®. Junctional Epidermolysis Bullosa. 4. National Organization for Rare Disorders (NORD). Laryngo-Onycho-Cutaneous Syndrome. <a href="https://rarediseases.org/rare-diseases/laryngo-onycho-cutaneous-syndrome/" target="_blank">https://rarediseases.org/rare-diseases/laryngo-onycho-cutaneous-syndrome/</a> 5. McLean WHI, et al. Mutations in LAMA3 cause Laryngo-Onycho-Cutaneous Syndrome. American Journal of Human Genetics. https://wevird.com/example-project-1 2026-07-25T08:21:33+00:00 always 0.5 https://freight.cargo.site/t/original/i/U3018194343955501035758757063282/ig-copy.jpg https://freight.cargo.site/t/original/i/L3018195463543739101412573293170/ig-6copy.jpg https://freight.cargo.site/t/original/i/Y3018195463562185845486282844786/ig2-copy.jpg https://freight.cargo.site/t/original/i/B3018195463599079333633701948018/ig5-copy.jpg https://freight.cargo.site/t/original/i/F3018195463433058636970315983474/ig-4copy.jpg https://freight.cargo.site/t/original/i/O3018195463580632589559992396402/ig3-copy.jpg https://wevird.com/camp 2026-07-26T19:31:49+00:00 always 0.5 https://freight.cargo.site/t/original/i/U3018194343955501035758757063282/ig-copy.jpg https://freight.cargo.site/t/original/i/U3053412464347627907823549524594/camp.png https://freight.cargo.site/t/original/i/W3053418348213351378590680722034/Open-Call-copy-2.jpg https://wevird.com/poli 2026-07-26T17:19:12+00:00 always 0.5 https://freight.cargo.site/t/original/i/U3018194343955501035758757063282/ig-copy.jpg https://freight.cargo.site/t/original/i/J3018383042876414455435252705906/ig3-p-copy.jpg https://freight.cargo.site/t/original/i/Q3018383042636606782477028534898/ig-p-copy.jpg https://freight.cargo.site/t/original/i/R3018383042857967711361543154290/ig2-p-copy.jpg https://freight.cargo.site/t/original/i/O3018385932060811512046355458674/Polly3-copy.jpg https://freight.cargo.site/t/original/i/N3053234820246843213028274973298/Polli-W.png https://freight.cargo.site/t/original/i/U3053239147244260350856668883570/3-copy.jpg 1. Orphanet. Polyrrhinia. <a href="https://www.orpha.net" target="_blank">https://www.orpha.net</a> 2. National Organization for Rare Disorders (NORD). Polyrrhinia. <a href="https://rarediseases.org/" target="_blank">https://rarediseases.org/</a> 3. Brucker MJ, Patel J, Sullivan PK. Polyrrhinia: Case Report and Embryologic Considerations. Plastic and Reconstructive Surgery. 17440364/"> 4. Turgut G, et al. Polyrrhinia: A Rare Congenital Craniofacial Malformation. Journal of Craniofacial Surgery. 5. National Center for Biotechnology Information (NCBI). Polyrrhinia: Case Reports and Literature Review. https://pubmed.ncbi.nlm.nih.gov/ https://wevird.com/ncs 2026-07-26T17:19:12+00:00 always 0.5 https://freight.cargo.site/t/original/i/H3018372946715128497165719546482/NCS.jpg https://freight.cargo.site/t/original/i/M3018377269912516355809945823858/web-ncs.jpg https://freight.cargo.site/t/original/i/W3053247922286629238195534408306/NCS-W.png https://freight.cargo.site/t/original/i/Z3053250078877032151505504283250/NCS.jpg https://wevird.com/mrkh 2026-07-26T17:36:57+00:00 always 0.5 https://freight.cargo.site/t/original/i/K3018342852936654320361437375090/mrkh.jpg https://freight.cargo.site/t/original/i/J3018361688999261705553140230770/MRKH-poster-copy.jpg <a href="https://porphyriafoundation.org/for-patients/types-of-porphyria/aip/" target="_blank">1. Orphanet. Mayer-Rokitansky-Küster-Hauser Syndrome. </a><a href="https://www.orpha.net/en/disease/detail/3109" target="_blank">https://www.orpha.net/en/disease/detail/3109</a> 2. GeneReviews®. Mayer-Rokitansky-Küster-Hauser Syndrome. 3. MedlinePlus Genetics. Mayer-Rokitansky-Küster-Hauser Syndrome. 4. National Organization for Rare Disorders (NORD). Mayer-Rokitansky-Küster-Hauser Syndrome. <a href="https://rarediseases.org/rare-diseases/mayer-rokitansky-kuster-hauser-syndrome/" target="_blank">https://rarediseases.org/rare-diseases/mayer-rokitansky-kuster-hauser-syndrome/</a> 5. American College of Obstetricians and Gynecologists (ACOG). Müllerian Agenesis: Diagnosis, Management, and Treatment. <a href="https://www.acog.org/clinical/clinical-guidance/committee-opinion/articles/2018/01/mullerian-agenesis-diagnosis-management-and-treatment" target="_blank">https://www.acog.org/clinical/clinical-guidance/committee-opinion/articles/2018/01/mullerian-agenesis-diagnosis-management-and-treatment</a> https://freight.cargo.site/t/original/i/D3053282693956486322931301329522/MRKH.png https://wevird.com/example-project-maffucci 2026-07-26T17:19:11+00:00 always 0.5 https://freight.cargo.site/t/original/i/U3018194343955501035758757063282/ig-copy.jpg https://freight.cargo.site/t/original/i/Y3018316499659816201864065034866/webbbbbb.jpg https://freight.cargo.site/t/original/i/Q3019932355193460617929392892530/maffucci-copy.jpg 1. Orphanet. Maffucci Syndrome. <a href="https://www.orpha.net/en/disease/detail/163634" target="_blank">https://www.orpha.net/en/disease/detail/163634</a> 2. MedlinePlus Genetics. Maffucci Syndrome. 3. GeneReviews®. Enchondromatosis Overview. 4. National Organization for Rare Disorders (NORD). Maffucci Syndrome. <a href="https://rarediseases.org/rare-diseases/maffucci-syndrome/" target="_blank">https://rarediseases.org/rare-diseases/maffucci-syndrome/</a> 5. Pansuriya TC, van Eijk R, d'Adamo P, et al. Somatic Mosaic IDH1 and IDH2 Mutations Are Associated with Enchondroma and Spindle Cell Hemangioma in Maffucci Syndrome. *Nature Genetics.* 2011. https://freight.cargo.site/t/original/i/A3053272890194540677031870835314/maffucci-w.png https://wevird.com/example-project-lam 2026-07-26T17:19:10+00:00 always 0.5 https://freight.cargo.site/t/original/i/U3018194343955501035758757063282/ig-copy.jpg https://freight.cargo.site/t/original/i/L3018306570902732712508712790642/Lam-Poster-info-copy-WEB.jpg https://freight.cargo.site/t/original/i/S3019925045541994202003598191218/lamc.jpg https://freight.cargo.site/t/original/i/X3053269953731138559503187290738/LAM-1-copy.jpg 1. Orphanet. Lymphangioleiomyomatosis. <a href="https://www.orpha.net/en/disease/detail/538" target="_blank">https://www.orpha.net/en/disease/detail/538</a> 2. GeneReviews®. Tuberous Sclerosis Complex. 3. MedlinePlus Genetics. Lymphangioleiomyomatosis. 4. The LAM Foundation. <a href="https://www.thelamfoundation.org/" target="_blank">https://www.thelamfoundation.org/</a> 5. Gupta N, Finlay GA, Kotloff RM, et al. Lymphangioleiomyomatosis Diagnosis and Management: High-Resolution Clinical Practice Guideline. American Thoracic Society. 2017. <a href="https://www.atsjournals.org/doi/full/10.1164/rccm.201607-1384ST" target="_blank">https://www.atsjournals.org/doi/full/10.1164/rccm.201607-1384ST</a> https://wevird.com/example-project-fop 2026-07-27T20:35:54+00:00 always 0.5 https://freight.cargo.site/t/original/i/U3055078839757906063353373502066/fop-b.jpg https://freight.cargo.site/t/original/i/J3055085188868961817149106006642/FOP-Infographic-copy.jpg https://freight.cargo.site/t/original/i/F3055085188739834608633139145330/FOP-2-copy.jpg 1. Orphanet. Fibrodysplasia Ossificans Progressiva. <a href="https://www.orpha.net/en/disease/detail/337" target="_blank">https://www.orpha.net/en/disease/detail/337</a> 2. GeneReviews®. Fibrodysplasia Ossificans Progressiva. "> 3. MedlinePlus Genetics. Fibrodysplasia Ossificans Progressiva. 4. International FOP Association (IFOPA). <a href="https://www.ifopa.org/" target="_blank">https://www.ifopa.org/</a> 5. Kaplan FS, Shore EM, Pignolo RJ. Fibrodysplasia Ossificans Progressiva. GeneReviews®. University of Washington, Seattle. https://www.ncbi.nlm.nih.gov/books/NBK558090/ https://wevird.com/example-project-cdg 2026-07-27T19:22:59+00:00 always 0.5 https://freight.cargo.site/t/original/i/U3018194343955501035758757063282/ig-copy.jpg https://freight.cargo.site/t/original/i/B3018218207327717573088271379058/CDG-poster-copy-web.jpg https://freight.cargo.site/t/original/i/L3054998866333944713322003147378/CDG-B.jpg https://freight.cargo.site/t/original/i/X3055004531808665095441752762994/33333.jpg 1. Orphanet. Congenital Disorder of Glycosylation (CDG). <a href="https://www.orpha.net/en/disease/detail/137" target="_blank">https://www.orpha.net/en/disease/detail/137</a> 2. Chang IJ, He M, Lam CT. Congenital Disorders of Glycosylation. Annals of Translational Medicine. 2018;6(24):477. 3. Lipiński P, Tylki-Szymańska A. Congenital Disorders of Glycosylation: What Clinicians Need to Know? Frontiers in Pediatrics. 2021;9:715151. <a href="https://www.frontiersin.org/articles/10.3389/fped.2021.715151/full" target="_blank">https://www.frontiersin.org/articles/10.3389/fped.2021.715151/full</a> 4. GeneReviews®. Congenital Disorders of Glycosylation Overview. University of Washington, Seattle. 5. Marques-da-Silva D, et al. Congenital Disorders of Glycosylation (CDG): State of the Art in 2023. Orphanet Journal of Rare Diseases. <a href="https://www.springermedizin.de/congenital-disorders-of-glycosylation-cdg-state-of-the-art-in-20/26202212" target="_blank">https://www.springermedizin.de/congenital-disorders-of-glycosylation-cdg-state-of-the-art-in-20/26202212</a> https://wevird.com/information 2026-07-26T17:36:56+00:00 always 0.5 https://freight.cargo.site/t/original/i/P2843050554633737056028031691378/we-vird-logo.png https://freight.cargo.site/t/original/i/E3051229712624695310377896356466/1.jpg https://wevird.com/header-(desktop) 2026-07-27T12:33:27+00:00 always 0.5 https://freight.cargo.site/t/original/i/L3019753848965644894244514015858/logo-alone.png https://freight.cargo.site/t/original/i/W3019755539701972970093467380338/yt5s.io-Virus--bacteria-and-coronavirus-disease-in-microsco.mp4 https://freight.cargo.site/t/original/i/K3019772348043131540910127950450/Banner4-copy.jpg https://freight.cargo.site/t/original/i/U3019772347858664100173032434290/Banner2-copy.jpg https://freight.cargo.site/t/original/i/C3019773646896828514873366784626/3-copy.jpg https://wevird.com/header-(mobile) 2026-07-25T08:21:33+00:00 always 0.5