All individuals with variants in gene MC2R

5 entries on 1 page. Showing entries 1 - 5.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00050538 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? microcephaly, muscular hypotonia, short philtrum, upslanted palpebral fissure 1 1 Johan den Dunnen
00291911 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00316036 - - unaffected heterozygous carrier parents F no China Chinese,Han - - - hydrocortisone GCCD1 hyperpigmentation 1 1 Wenjuan Qiu
00384654 #1 - - M ? Italy - - - - - GCCD1 very high levels of ACTH 1 1 Annalaura Torella
00444488 Pat96 PubMed: Duan 2023 patient - - China - - - - - adrenal hyperplasia hyperpigmentation; tall stature; no hyponatremia; no hyperkalemia; hypoglycemia; no elevated 17OHP 1 1 Johan den Dunnen
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