All individuals with variants in gene C19orf44

14 entries on 1 page. Showing entries 1 - 14.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00452915 TB752 PubMed: Ehrenberg 2025 3-generation family, 1 affected, unaffected parents M yes Israel Yemenite Jewish - - - - RD - 1 1 Tamar Ben-Yosef
00452916 TB1002 PubMed: Ehrenberg 2025 2-generation family, 1 affected, unaffected parents M no Israel Yemenite Jewish - - - - RD - 1 1 Tamar Ben-Yosef
00452917 TB777 PubMed: Ehrenberg 2025 2-generation family, 1 affected, unaffected parents M no Israel Ashkenazi Jewish - - - - RD - 1 1 Tamar Ben-Yosef
00452918 MOL311 PubMed: Ehrenberg 2025 3-generation family, 1 affected, unaffected parents M yes Israel Ashkenazi Jewish - - - - RD - 1 1 Tamar Ben-Yosef
00452919 MOL2388 PubMed: Ehrenberg 2025 2-generation family, 1 affected, unaffected parents F no Israel Yemenite Jewish - - - - RD - 1 1 Tamar Ben-Yosef
00452920 TB1441-1 PubMed: Ehrenberg 2025 2-generation family, 3 affected sisters, unaffected parents F no Israel Yemenite Jewish - - - - RD - 1 3 Tamar Ben-Yosef
00452921 TB1334 PubMed: Ehrenberg 2025 2-generation family, 1 affected, unaffected parents M no Israel Yemenite Jewish - - - - RD - 1 1 Tamar Ben-Yosef
00452922 GC22684 PubMed: Ehrenberg 2025 2-generation family, 1 affected, unaffected parents M yes Iran - - - - - RD - 1 1 Tamar Ben-Yosef
00452923 GC32213 PubMed: Ehrenberg 2025 2-generation family, 1 affected, unaffected parents F no Iraq Kurdish - - - - RD - 2 1 Tamar Ben-Yosef
00452924 GC20987 PubMed: Ehrenberg 2025 2-generation family, 1 affected, unaffected parents M no United Kingdom (Great Britain) - - - - - RD - 2 1 Tamar Ben-Yosef
00464580 OGI838 PubMed: Ehrenberg 2025 2-generation family, 3 affected (2f, M), unaffected parents F;M - United States jew-Ashkenazi - - - - RD - 1 3 Johan den Dunnen
00467807 Pat1 PubMed: Hussain 2025 3-generation family, 1 affected, unaffected heterozygous carrier parents F - - Europe - - - - macular dystrophy see paper; ..., 40s-central vision loss, more pronounced left eye (led to legal blindness, cessation of driving); fundus central chorioretinal atrophy with flecks,RPE mottling; bilateral central scotomas; hypoautofluorescence patches, complete ring of peripapillary atrophy and nasal sparing; severe atrophy both retina/choroid through macula; multifocal ERG severely abnormal, amplitude both eyes; hypertension;full-field ERG moderate reduction rod-driven responses/cone responses; gout; grandparents/father glaucoma 1 1 Johan den Dunnen
00467808 Pat2 PubMed: Hussain 2025 3-generation family, 1 affected, unaffected heterozygous carrier parents M yes - Middle-East - - - - macular dystrophy see paper; ..., Stargardt-like disease; fundus notable progression paracentral geographic atrophy; autofluorescence significant progression paracentral geographic atrophy; progressive paracentral geographic atrophy; renal cell cancer 1 1 Johan den Dunnen
00467809 Pat3 PubMed: Hussain 2025 3-generation family, 1 affected, unaffected heterozygous carrier parents F no - Asia-E - - - - macular dystrophy see paper; ..., central blurriness, difficulty seeing in dim light; constricted visual acuity; macular geographic atrophy and granular RPE changes out to the periphery; retinal thinning; full field ERG severely reduced responses in scotopic/photopic waveforms; pseudophakia, hypertension and anaemia 2 1 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.