All individuals with variants in gene SAMD9

3 entries on 1 page. Showing entries 1 - 3.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00397591 Fam1;FamPatII2 PubMed: Topaz 2006, PubMed: Chefetz 2008 2-generation family, 2 affected sibs, unaffected heterozygous carrier parents; maternal grandparents Jewish-Yemenite origin, paternal grandmother/paternal grandfather Jewish-Moroccan origin M ? Israel Jewish-Yemenite;Jewish-Morocco - - - - NFTC Retinopathy of prematurity: HP:0500049: Subcutaneous nodule HP:0001482: Edema HP:0000969: Erythema HP:0010783: Gingivitis HP:0000230 2 2 Litika Vermani
00397592 FamPatII1 PubMed: Chefetz 2008 sister F ? Israel Jewish-Yemenite;Jewish-Morocco - - - - NFTC Retinopathy of prematurity (HP:0500049), Subcutaneous calcification (HP:0007618), Edema (HP:0000969), Erythema (HP:0010783), Abnormal pigmentation of the oral mucosa (HP:0100669), Gingivitis (HP:0000230) 2 1 Litika Vermani
00444485 Pat93 PubMed: Duan 2023 patient - - China - - - - - adrenal hyperplasia dehydration; intrauterine growth retardation; asphyxia neonatorum; convulsions; infections; MODS; hyponatremia; hyperkalemia; hypoglycemia; no elevated 17OHP 1 1 Johan den Dunnen
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